Canonical Allele Identifier: CA51356522

Gene: REEP1

Linked Data

• ClinVar Variation Id: 994781
• ClinVar RCV Id: RCV001288448
• dbSNP Id: rs904027097
• gnomAD v2: 2-86444080-C-T
• gnomAD v3: 2-86216957-C-T
• gnomAD v4: 2-86216957-C-T
• MyVariant Identifiers: chr2:g.86444080C>T (hg19) ; chr2:g.86216957C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.86216957C>T , CM000664.2:g.86216957C>T	GRCh38
NC_000002.11:g.86444080C>T , CM000664.1:g.86444080C>T	GRCh37
NC_000002.10:g.86297591C>T	NCBI36
NG_013037.1:g.126127G>A , LRG_713:g.126127G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000643817.2:c.*82G>A	ENSP00000495610.2:n.*82G>A
ENST00000686220.1:c.*197G>A	ENSP00000509904.1:n.*197G>A
ENST00000687696.1:n.279G>A
ENST00000687927.1:n.1215G>A
ENST00000688400.1:c.437G>A	ENSP00000510490.1:n.437G>A
ENST00000689156.1:c.*82G>A	ENSP00000509143.1:n.*82G>A
ENST00000691093.1:c.*143G>A	ENSP00000509465.1:n.*143G>A
ENST00000691703.1:c.*143G>A	ENSP00000508496.1:n.*143G>A
ENST00000692664.1:c.*143G>A	ENSP00000508656.1:n.*143G>A
ENST00000693329.1:c.*223G>A	ENSP00000508490.1:n.*223G>A
ENST00000453231.6:c.*143G>A	ENSP00000392197.2:n.*143G>A
ENST00000535845.6:c.*143G>A	ENSP00000437567.1:n.*143G>A
ENST00000538924.7:c.*82G>A MANE Select	ENSP00000438346.3:n.*82G>A
ENST00000541910.6:c.*82G>A	ENSP00000442681.1:n.*82G>A
ENST00000642243.1:c.1045G>A	ENSP00000494960.1:n.1045G>A
ENST00000643817.1:c.859G>A	ENSP00000495610.1:n.859G>A
ENST00000644644.1:c.946G>A	ENSP00000494305.1:n.946G>A
ENST00000646181.1:n.622G>A
ENST00000165698.9:c.*143G>A	ENSP00000165698.5:n.*143G>A
ENST00000535845.5:c.*143G>A	ENSP00000437567.1:n.*143G>A
ENST00000538924.5:c.*143G>A	ENSP00000438346.1:n.*143G>A
ENST00000541910.5:c.*82G>A	ENSP00000442681.1:n.*82G>A
NM_001164730.1:c.*143G>A , LRG_713t1:c.*143G>A	NP_001158202.1:n.*143G>A
NM_001164731.1:c.*143G>A	NP_001158203.1:n.*143G>A
NM_001164732.1:c.*82G>A	NP_001158204.1:n.*82G>A
NM_022912.2:c.*143G>A , LRG_713t2:c.*143G>A	NP_075063.1:n.*143G>A
XM_005264502.1:c.*82G>A	XP_005264559.1:n.*82G>A
XM_005264504.1:c.*82G>A	XP_005264561.1:n.*82G>A
XM_011533043.1:c.*82G>A	XP_011531345.1:n.*82G>A
XM_011533044.1:c.*82G>A	XP_011531346.1:n.*82G>A
XM_011533045.1:c.*82G>A	XP_011531347.1:n.*82G>A
XM_005264502.2:c.*82G>A	XP_005264559.1:n.*82G>A
XM_011533045.2:c.*82G>A	XP_011531347.1:n.*82G>A
XM_017004725.1:c.*82G>A	XP_016860214.1:n.*82G>A
XM_017004726.1:c.*143G>A	XP_016860215.1:n.*143G>A
XM_017004727.1:c.*143G>A	XP_016860216.1:n.*143G>A
NM_001164730.2:c.*143G>A	NP_001158202.1:n.*143G>A
NM_001164731.2:c.*143G>A	NP_001158203.1:n.*143G>A
NM_001164732.2:c.*82G>A	NP_001158204.1:n.*82G>A
NM_001371279.1:c.*82G>A MANE Select	NP_001358208.1:n.*82G>A
NM_001371280.1:c.*82G>A	NP_001358209.1:n.*82G>A
NM_022912.3:c.*143G>A	NP_075063.1:n.*143G>A