Canonical Allele Identifier: CA1519938527

Gene: F11

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186285740T= , CM000666.2:g.186285740T=	GRCh38
NC_000004.11:g.187206894T= , CM000666.1:g.187206894T=	GRCh37
NC_000004.10:g.187443888T=	NCBI36
NG_008051.1:g.24777T= , LRG_583:g.24777T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1407T= MANE Select	ENSP00000384957.2:p.His469=
ENST00000264691.4:c.103T=
ENST00000264692.8:c.1245T=	ENSP00000264692.5:p.His415=
ENST00000403665.6:c.1407T=	ENSP00000384957.2:p.His469=
NM_000128.3:c.1407T= , LRG_583t1:c.1407T=	NP_000119.1:p.His469=
XM_005262821.2:c.1410T=	XP_005262878.1:p.His470=
XM_005262822.2:c.1410T=	XP_005262879.1:p.His470=
XM_005262823.2:c.1140T=	XP_005262880.1:p.His380=
XM_005262824.1:c.1410T=	XP_005262881.1:p.His470=
XM_006714137.1:c.1362T=	XP_006714200.1:p.His454=
XR_938706.1:n.1815T=
XR_938707.1:n.1815T=
XM_005262821.4:c.1410T=	XP_005262878.1:p.His470=
XM_005262822.4:c.1410T=	XP_005262879.1:p.His470=
XM_005262823.4:c.1140T=	XP_005262880.1:p.His380=
XM_006714137.3:c.1362T=	XP_006714200.1:p.His454=
XR_001741172.2:n.1881T=
NM_000128.4:c.1407T= MANE Select	NP_000119.1:p.His469=