Canonical Allele Identifier: CA358938616
Gene: F11 HGNC NCBI

Linked Data

dbSNP Id: rs1423578143

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186280476G>A , CM000666.2:g.186280476G>A GRCh38
NC_000004.11:g.187201630G>A , CM000666.1:g.187201630G>A GRCh37
NC_000004.10:g.187438624G>A NCBI36
NG_008051.1:g.19513G>A , LRG_583:g.19513G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000403665.7:c.1031G>A MANE Select ENSP00000384957.2:p.Gly344Asp
ENST00000264692.8:c.869G>A ENSP00000264692.5:p.Gly290Asp
ENST00000403665.6:c.1031G>A ENSP00000384957.2:p.Gly344Asp
ENST00000452239.1:c.478G>A
NM_000128.3:c.1031G>A , LRG_583t1:c.1031G>A NP_000119.1:p.Gly344Asp
XM_005262821.2:c.1034G>A XP_005262878.1:p.Gly345Asp
XM_005262822.2:c.1034G>A XP_005262879.1:p.Gly345Asp
XM_005262823.2:c.764G>A XP_005262880.1:p.Gly255Asp
XM_005262824.1:c.1034G>A XP_005262881.1:p.Gly345Asp
XM_006714137.1:c.986G>A XP_006714200.1:p.Gly329Asp
XR_938706.1:n.1386G>A
XR_938707.1:n.1386G>A
XM_005262821.4:c.1034G>A XP_005262878.1:p.Gly345Asp
XM_005262822.4:c.1034G>A XP_005262879.1:p.Gly345Asp
XM_005262823.4:c.764G>A XP_005262880.1:p.Gly255Asp
XM_006714137.3:c.986G>A XP_006714200.1:p.Gly329Asp
XM_017007884.2:c.1034G>A XP_016863373.1:p.Gly345Asp
XM_017007885.2:c.1034G>A XP_016863374.1:p.Gly345Asp
XM_017007886.2:c.1031G>A XP_016863375.1:p.Gly344Asp
XR_001741172.2:n.1452G>A
NM_000128.4:c.1031G>A MANE Select NP_000119.1:p.Gly344Asp