Canonical Allele Identifier: CA1519937814
Gene: F11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186284229T= , CM000666.2:g.186284229T= GRCh38
NC_000004.11:g.187205383T= , CM000666.1:g.187205383T= GRCh37
NC_000004.10:g.187442377T= NCBI36
NG_008051.1:g.23266T= , LRG_583:g.23266T=

Transcript Alleles

HGVS Amino-acid change
ENST00000403665.7:c.1273T= MANE Select ENSP00000384957.2:p.Trp425=
ENST00000264692.8:c.1111T= ENSP00000264692.5:p.Trp371=
ENST00000403665.6:c.1273T= ENSP00000384957.2:p.Trp425=
NM_000128.3:c.1273T= , LRG_583t1:c.1273T= NP_000119.1:p.Trp425=
XM_005262821.2:c.1276T= XP_005262878.1:p.Trp426=
XM_005262822.2:c.1276T= XP_005262879.1:p.Trp426=
XM_005262823.2:c.1006T= XP_005262880.1:p.Trp336=
XM_005262824.1:c.1276T= XP_005262881.1:p.Trp426=
XM_006714137.1:c.1228T= XP_006714200.1:p.Trp410=
XR_938706.1:n.1681T=
XR_938707.1:n.1681T=
XM_005262821.4:c.1276T= XP_005262878.1:p.Trp426=
XM_005262822.4:c.1276T= XP_005262879.1:p.Trp426=
XM_005262823.4:c.1006T= XP_005262880.1:p.Trp336=
XM_006714137.3:c.1228T= XP_006714200.1:p.Trp410=
XR_001741172.2:n.1747T=
NM_000128.4:c.1273T= MANE Select NP_000119.1:p.Trp425=