Canonical Allele Identifier: CA348778793

Gene: NEB RIF1

Linked Data

• MyVariant Identifiers: chr2:g.152354159T>G (hg19) ; chr2:g.151497645T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.151497645T>G , CM000664.2:g.151497645T>G	GRCh38
NC_000002.11:g.152354159T>G , CM000664.1:g.152354159T>G	GRCh37
NC_000002.10:g.152062405T>G	NCBI36
NG_009382.2:g.241843A>C , LRG_202:g.241843A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000434685.6:c.3075-5151A>C (NEB)
ENST00000688578.1:c.900-612A>C (NEB)
ENST00000690043.1:c.6378-3392A>C (NEB)
ENST00000693000.1:n.2657-5151A>C (NEB)
ENST00000397345.8:c.24281A>C (NEB) MANE Select	ENSP00000380505.3:p.Asn8094Thr
ENST00000427231.7:c.24281A>C (NEB) MANE Plus Clinical	ENSP00000416578.2:p.Asn8094Thr
ENST00000172853.14:c.18826-1277A>C (NEB)	ENSP00000172853.10:n.18826-1277A>C
ENST00000397337.6:c.682A>C (NEB)
ENST00000397345.7:c.24281A>C (NEB)	ENSP00000380505.3:p.Asn8094Thr
ENST00000409198.5:c.18826-1277A>C (NEB)	ENSP00000386259.1:n.18826-1277A>C
ENST00000413693.5:c.8026-1277A>C (NEB)	ENSP00000410961.1:n.8026-1277A>C
ENST00000421461.6:c.717A>C (NEB)
ENST00000424585.1:c.610-612A>C (NEB)	ENSP00000404876.1:n.610-612A>C
ENST00000427231.6:c.24281A>C (NEB)	ENSP00000416578.2:p.Asn8094Thr
ENST00000434685.5:c.1395-3392A>C (NEB)
ENST00000454583.6:c.2754-1700T>G (RIF1)
ENST00000457745.1:n.579-141T>G (RIF1)
ENST00000484077.1:n.353-141T>G (RIF1)
ENST00000498015.2:n.226-5151A>C (NEB)
ENST00000603639.5:c.24281A>C (NEB)	ENSP00000473894.1:p.Asn8094Thr
ENST00000604864.5:c.24281A>C (NEB)	ENSP00000474498.1:p.Asn8094Thr
ENST00000618972.4:c.24386A>C (NEB)	ENSP00000484342.1:p.Asn8129Thr
NM_001164507.1:c.24281A>C (NEB)	NP_001157979.1:p.Asn8094Thr
NM_001164508.1:c.24281A>C (NEB)	NP_001157980.1:p.Asn8094Thr
NM_001271208.1:c.24386A>C , LRG_202t1:c.24386A>C (NEB)	NP_001258137.1:p.Asn8129Thr
NM_004543.4:c.18826-1277A>C (NEB)	NP_004534.2:n.18826-1277A>C
XM_005246590.1:c.24188A>C (NEB)	XP_005246647.1:p.Asn8063Thr
XM_005246591.1:c.24188A>C (NEB)	XP_005246648.1:p.Asn8063Thr
XM_005246592.1:c.24281A>C (NEB)	XP_005246649.1:p.Asn8094Thr
XM_005246593.1:c.24281A>C (NEB)	XP_005246650.1:p.Asn8094Thr
XM_005246594.1:c.24188A>C (NEB)	XP_005246651.1:p.Asn8063Thr
XM_005246595.1:c.24188A>C (NEB)	XP_005246652.1:p.Asn8063Thr
XM_005246596.1:c.24095A>C (NEB)	XP_005246653.1:p.Asn8032Thr
XM_005246597.1:c.24281A>C (NEB)	XP_005246654.1:p.Asn8094Thr
XM_005246598.1:c.24281A>C (NEB)	XP_005246655.1:p.Asn8094Thr
XM_005246599.1:c.24002A>C (NEB)	XP_005246656.1:p.Asn8001Thr
XM_005246600.1:c.24002A>C (NEB)	XP_005246657.1:p.Asn8001Thr
XM_005246601.1:c.23929-612A>C (NEB)	XP_005246658.1:n.23929-612A>C
XM_005246602.1:c.23909A>C (NEB)	XP_005246659.1:p.Asn7970Thr
XM_005246603.1:c.23929-1277A>C (NEB)	XP_005246660.1:n.23929-1277A>C
XM_005246604.1:c.23929-612A>C (NEB)	XP_005246661.1:n.23929-612A>C
XM_005246606.1:c.23909A>C (NEB)	XP_005246663.1:p.Asn7970Thr
XM_005246608.1:c.23929-3392A>C (NEB)	XP_005246665.1:n.23929-3392A>C
XM_005246610.1:c.23836-3392A>C (NEB)	XP_005246667.1:n.23836-3392A>C
XM_005246611.1:c.24021+3746A>C (NEB)	XP_005246668.1:n.24021+3746A>C
XM_005246612.1:c.23552A>C (NEB)	XP_005246669.1:p.Asn7851Thr
XM_005246613.1:c.23552A>C (NEB)	XP_005246670.1:p.Asn7851Thr
XM_005246615.1:c.23909A>C (NEB)	XP_005246672.1:p.Asn7970Thr
XM_005246616.1:c.*579A>C (NEB)	XP_005246673.1:n.*579A>C
XM_005246617.1:c.21365A>C (NEB)	XP_005246674.1:p.Asn7122Thr
XM_006712541.1:c.23929-1277A>C (NEB)	XP_006712604.1:n.23929-1277A>C
XM_006712542.1:c.24002A>C (NEB)	XP_006712605.1:p.Asn8001Thr
XM_011511224.1:c.24188A>C (NEB)	XP_011509526.1:p.Asn8063Thr
XM_011511225.1:c.23743-3392A>C (NEB)	XP_011509527.1:n.23743-3392A>C
XM_011511226.1:c.22094A>C (NEB)	XP_011509528.1:p.Asn7365Thr
XM_011511227.1:c.19907A>C (NEB)	XP_011509529.1:p.Asn6636Thr
XR_922955.1:n.7838+14310T>G (RIF1)
XR_922956.1:n.7937-141T>G (RIF1)
XR_922957.1:n.7839-141T>G (RIF1)
XM_005246590.2:c.24188A>C (NEB)	XP_005246647.1:p.Asn8063Thr
XM_005246591.2:c.24188A>C (NEB)	XP_005246648.1:p.Asn8063Thr
XM_005246592.2:c.24281A>C (NEB)	XP_005246649.1:p.Asn8094Thr
XM_005246593.2:c.24281A>C (NEB)	XP_005246650.1:p.Asn8094Thr
XM_005246594.2:c.24188A>C (NEB)	XP_005246651.1:p.Asn8063Thr
XM_005246596.2:c.24095A>C (NEB)	XP_005246653.1:p.Asn8032Thr
XM_005246597.2:c.24281A>C (NEB)	XP_005246654.1:p.Asn8094Thr
XM_005246598.2:c.24281A>C (NEB)	XP_005246655.1:p.Asn8094Thr
XM_005246599.2:c.24002A>C (NEB)	XP_005246656.1:p.Asn8001Thr
XM_005246601.2:c.23929-612A>C (NEB)	XP_005246658.1:n.23929-612A>C
XM_005246602.2:c.23909A>C (NEB)	XP_005246659.1:p.Asn7970Thr
XM_005246603.2:c.23929-1277A>C (NEB)	XP_005246660.1:n.23929-1277A>C
XM_005246604.2:c.23929-612A>C (NEB)	XP_005246661.1:n.23929-612A>C
XM_005246606.2:c.23909A>C (NEB)	XP_005246663.1:p.Asn7970Thr
XM_005246608.2:c.23929-3392A>C (NEB)	XP_005246665.1:n.23929-3392A>C
XM_005246610.2:c.23836-3392A>C (NEB)	XP_005246667.1:n.23836-3392A>C
XM_005246611.2:c.24021+3746A>C (NEB)	XP_005246668.1:n.24021+3746A>C
XM_005246612.2:c.23552A>C (NEB)	XP_005246669.1:p.Asn7851Thr
XM_005246613.2:c.23552A>C (NEB)	XP_005246670.1:p.Asn7851Thr
XM_005246615.2:c.23909A>C (NEB)	XP_005246672.1:p.Asn7970Thr
XM_005246617.2:c.21365A>C (NEB)	XP_005246674.1:p.Asn7122Thr
XM_006712541.2:c.23929-1277A>C (NEB)	XP_006712604.1:n.23929-1277A>C
XM_006712542.2:c.24002A>C (NEB)	XP_006712605.1:p.Asn8001Thr
XM_011511225.2:c.23743-3392A>C (NEB)	XP_011509527.1:n.23743-3392A>C
XM_011511226.2:c.22094A>C (NEB)	XP_011509528.1:p.Asn7365Thr
XM_011511227.2:c.19907A>C (NEB)	XP_011509529.1:p.Asn6636Thr
XM_017004177.1:c.24170A>C (NEB)	XP_016859666.1:p.Asn8057Thr
XM_017004178.1:c.24095A>C (NEB)	XP_016859667.1:p.Asn8032Thr
XM_017004179.1:c.23836-612A>C (NEB)	XP_016859668.1:n.23836-612A>C
XM_017004180.1:c.23816A>C (NEB)	XP_016859669.1:p.Asn7939Thr
XM_017004181.1:c.23836-1277A>C (NEB)	XP_016859670.1:n.23836-1277A>C
XM_017004182.1:c.23836-1277A>C (NEB)	XP_016859671.1:n.23836-1277A>C
XM_017004183.1:c.23836-3392A>C (NEB)	XP_016859672.1:n.23836-3392A>C
XM_017004184.1:c.23836-1277A>C (NEB)	XP_016859673.1:n.23836-1277A>C
XM_017004185.1:c.23743-5151A>C (NEB)	XP_016859674.1:n.23743-5151A>C
XR_001738811.2:n.8312-141T>G (RIF1)
XR_001738812.2:n.8312-1760T>G (RIF1)
XR_001738813.2:n.8214-141T>G (RIF1)
XR_001738814.2:n.8214-1760T>G (RIF1)
XR_001738815.2:n.8214-5389T>G (RIF1)
XR_001738816.2:n.8214-8565T>G (RIF1)
XR_001738817.2:n.8213+14310T>G (RIF1)
NM_001271208.2:c.24386A>C (NEB)	NP_001258137.2:p.Asn8129Thr
NM_004543.5:c.18826-1277A>C (NEB)	NP_004534.3:n.18826-1277A>C
NM_001164507.2:c.24281A>C (NEB) MANE Plus Clinical	NP_001157979.2:p.Asn8094Thr
NM_001164508.2:c.24281A>C (NEB) MANE Select	NP_001157980.2:p.Asn8094Thr