Canonical Allele Identifier: CA112102507
Gene: F11 HGNC NCBI

Linked Data

dbSNP Id: rs866457660

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186284217A>G , CM000666.2:g.186284217A>G GRCh38
NC_000004.11:g.187205371A>G , CM000666.1:g.187205371A>G GRCh37
NC_000004.10:g.187442365A>G NCBI36
NG_008051.1:g.23254A>G , LRG_583:g.23254A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000403665.7:c.1261A>G MANE Select ENSP00000384957.2:p.Ile421Val
ENST00000264692.8:c.1099A>G ENSP00000264692.5:p.Ile367Val
ENST00000403665.6:c.1261A>G ENSP00000384957.2:p.Ile421Val
NM_000128.3:c.1261A>G , LRG_583t1:c.1261A>G NP_000119.1:p.Ile421Val
XM_005262821.2:c.1264A>G XP_005262878.1:p.Ile422Val
XM_005262822.2:c.1264A>G XP_005262879.1:p.Ile422Val
XM_005262823.2:c.994A>G XP_005262880.1:p.Ile332Val
XM_005262824.1:c.1264A>G XP_005262881.1:p.Ile422Val
XM_006714137.1:c.1216A>G XP_006714200.1:p.Ile406Val
XR_938706.1:n.1669A>G
XR_938707.1:n.1669A>G
XM_005262821.4:c.1264A>G XP_005262878.1:p.Ile422Val
XM_005262822.4:c.1264A>G XP_005262879.1:p.Ile422Val
XM_005262823.4:c.994A>G XP_005262880.1:p.Ile332Val
XM_006714137.3:c.1216A>G XP_006714200.1:p.Ile406Val
XR_001741172.2:n.1735A>G
NM_000128.4:c.1261A>G MANE Select NP_000119.1:p.Ile421Val