Canonical Allele Identifier: CA3164029

Gene: F11 F11-AS1

Linked Data

• dbSNP Id: rs769022094
• ExAC: 4:187207703 T / C
• gnomAD v2: 4-187207703-T-C
• gnomAD v4: 4-186286549-T-C
• MyVariant Identifiers: chr4:g.187207703T>C (hg19) ; chr4:g.186286549T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186286549T>C , CM000666.2:g.186286549T>C	GRCh38
NC_000004.11:g.187207703T>C , CM000666.1:g.187207703T>C	GRCh37
NC_000004.10:g.187444697T>C	NCBI36
NG_008051.1:g.25586T>C , LRG_583:g.25586T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1576+39T>C (F11) MANE Select	ENSP00000384957.2:n.1576+39T>C
ENST00000264691.4:c.176+736T>C (F11)
ENST00000264692.8:c.1414+39T>C (F11)	ENSP00000264692.5:n.1414+39T>C
ENST00000403665.6:c.1576+39T>C (F11)	ENSP00000384957.2:n.1576+39T>C
NM_000128.3:c.1576+39T>C , LRG_583t1:c.1576+39T>C (F11)	NP_000119.1:n.1576+39T>C
NR_033900.1:n.1067-283A>G (F11-AS1)
XM_005262821.2:c.1579+39T>C (F11)	XP_005262878.1:n.1579+39T>C
XM_005262822.2:c.1483+736T>C (F11)	XP_005262879.1:n.1483+736T>C
XM_005262823.2:c.1309+39T>C (F11)	XP_005262880.1:n.1309+39T>C
XM_005262824.1:c.1487T>C (F11)	XP_005262881.1:p.Met496Thr
XM_006714137.1:c.1531+39T>C (F11)	XP_006714200.1:n.1531+39T>C
XR_938706.1:n.1984+39T>C (F11)
XR_938707.1:n.1888+736T>C (F11)
XM_005262821.4:c.1579+39T>C (F11)	XP_005262878.1:n.1579+39T>C
XM_005262822.4:c.1483+736T>C (F11)	XP_005262879.1:n.1483+736T>C
XM_005262823.4:c.1309+39T>C (F11)	XP_005262880.1:n.1309+39T>C
XM_006714137.3:c.1531+39T>C (F11)	XP_006714200.1:n.1531+39T>C
NM_000128.4:c.1576+39T>C (F11) MANE Select	NP_000119.1:n.1576+39T>C