Canonical Allele Identifier: CA1519938505
Gene: F11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186285687T= , CM000666.2:g.186285687T= GRCh38
NC_000004.11:g.187206841T= , CM000666.1:g.187206841T= GRCh37
NC_000004.10:g.187443835T= NCBI36
NG_008051.1:g.24724T= , LRG_583:g.24724T=

Transcript Alleles

HGVS Amino-acid change
ENST00000403665.7:c.1354T= MANE Select ENSP00000384957.2:p.Ser452=
ENST00000264691.4:c.50T=
ENST00000264692.8:c.1192T= ENSP00000264692.5:p.Ser398=
ENST00000403665.6:c.1354T= ENSP00000384957.2:p.Ser452=
NM_000128.3:c.1354T= , LRG_583t1:c.1354T= NP_000119.1:p.Ser452=
XM_005262821.2:c.1357T= XP_005262878.1:p.Ser453=
XM_005262822.2:c.1357T= XP_005262879.1:p.Ser453=
XM_005262823.2:c.1087T= XP_005262880.1:p.Ser363=
XM_005262824.1:c.1357T= XP_005262881.1:p.Ser453=
XM_006714137.1:c.1309T= XP_006714200.1:p.Ser437=
XR_938706.1:n.1762T=
XR_938707.1:n.1762T=
XM_005262821.4:c.1357T= XP_005262878.1:p.Ser453=
XM_005262822.4:c.1357T= XP_005262879.1:p.Ser453=
XM_005262823.4:c.1087T= XP_005262880.1:p.Ser363=
XM_006714137.3:c.1309T= XP_006714200.1:p.Ser437=
XR_001741172.2:n.1828T=
NM_000128.4:c.1354T= MANE Select NP_000119.1:p.Ser452=