Canonical Allele Identifier: CA1519937826

Gene: F11

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186284252T= , CM000666.2:g.186284252T=	GRCh38
NC_000004.11:g.187205406T= , CM000666.1:g.187205406T=	GRCh37
NC_000004.10:g.187442400T=	NCBI36
NG_008051.1:g.23289T= , LRG_583:g.23289T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000403665.7:c.1296T= MANE Select	ENSP00000384957.2:p.Cys432=
ENST00000264692.8:c.1134T=	ENSP00000264692.5:p.Cys378=
ENST00000403665.6:c.1296T=	ENSP00000384957.2:p.Cys432=
NM_000128.3:c.1296T= , LRG_583t1:c.1296T=	NP_000119.1:p.Cys432=
XM_005262821.2:c.1299T=	XP_005262878.1:p.Cys433=
XM_005262822.2:c.1299T=	XP_005262879.1:p.Cys433=
XM_005262823.2:c.1029T=	XP_005262880.1:p.Cys343=
XM_005262824.1:c.1299T=	XP_005262881.1:p.Cys433=
XM_006714137.1:c.1251T=	XP_006714200.1:p.Cys417=
XR_938706.1:n.1704T=
XR_938707.1:n.1704T=
XM_005262821.4:c.1299T=	XP_005262878.1:p.Cys433=
XM_005262822.4:c.1299T=	XP_005262879.1:p.Cys433=
XM_005262823.4:c.1029T=	XP_005262880.1:p.Cys343=
XM_006714137.3:c.1251T=	XP_006714200.1:p.Cys417=
XR_001741172.2:n.1770T=
NM_000128.4:c.1296T= MANE Select	NP_000119.1:p.Cys432=