Canonical Allele Identifier: CA3163817
Gene: F11 HGNC NCBI

Linked Data

ClinVar Variation Id: 3091393
ClinVar RCV Id: RCV004385779
dbSNP Id: rs773261994

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186280277A>T , CM000666.2:g.186280277A>T GRCh38
NC_000004.11:g.187201431A>T , CM000666.1:g.187201431A>T GRCh37
NC_000004.10:g.187438425A>T NCBI36
NG_008051.1:g.19314A>T , LRG_583:g.19314A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000403665.7:c.920A>T MANE Select ENSP00000384957.2:p.Asp307Val
ENST00000264692.8:c.758A>T ENSP00000264692.5:p.Asp253Val
ENST00000403665.6:c.920A>T ENSP00000384957.2:p.Asp307Val
ENST00000452239.1:c.367A>T
NM_000128.3:c.920A>T , LRG_583t1:c.920A>T NP_000119.1:p.Asp307Val
XM_005262821.2:c.920A>T XP_005262878.1:p.Asp307Val
XM_005262822.2:c.920A>T XP_005262879.1:p.Asp307Val
XM_005262823.2:c.650A>T XP_005262880.1:p.Asp217Val
XM_005262824.1:c.920A>T XP_005262881.1:p.Asp307Val
XM_006714137.1:c.872A>T XP_006714200.1:p.Asp291Val
XR_938706.1:n.1272A>T
XR_938707.1:n.1272A>T
XM_005262821.4:c.920A>T XP_005262878.1:p.Asp307Val
XM_005262822.4:c.920A>T XP_005262879.1:p.Asp307Val
XM_005262823.4:c.650A>T XP_005262880.1:p.Asp217Val
XM_006714137.3:c.872A>T XP_006714200.1:p.Asp291Val
XM_017007884.2:c.920A>T XP_016863373.1:p.Asp307Val
XM_017007885.2:c.920A>T XP_016863374.1:p.Asp307Val
XM_017007886.2:c.920A>T XP_016863375.1:p.Asp307Val
XR_001741172.2:n.1253A>T
NM_000128.4:c.920A>T MANE Select NP_000119.1:p.Asp307Val