Canonical Allele Identifier: CA1519937824

Gene: F11

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186284245C= , CM000666.2:g.186284245C=	GRCh38
NC_000004.11:g.187205399C= , CM000666.1:g.187205399C=	GRCh37
NC_000004.10:g.187442393C=	NCBI36
NG_008051.1:g.23282C= , LRG_583:g.23282C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000403665.7:c.1289C= MANE Select	ENSP00000384957.2:p.Ala430=
ENST00000264692.8:c.1127C=	ENSP00000264692.5:p.Ala376=
ENST00000403665.6:c.1289C=	ENSP00000384957.2:p.Ala430=
NM_000128.3:c.1289C= , LRG_583t1:c.1289C=	NP_000119.1:p.Ala430=
XM_005262821.2:c.1292C=	XP_005262878.1:p.Ala431=
XM_005262822.2:c.1292C=	XP_005262879.1:p.Ala431=
XM_005262823.2:c.1022C=	XP_005262880.1:p.Ala341=
XM_005262824.1:c.1292C=	XP_005262881.1:p.Ala431=
XM_006714137.1:c.1244C=	XP_006714200.1:p.Ala415=
XR_938706.1:n.1697C=
XR_938707.1:n.1697C=
XM_005262821.4:c.1292C=	XP_005262878.1:p.Ala431=
XM_005262822.4:c.1292C=	XP_005262879.1:p.Ala431=
XM_005262823.4:c.1022C=	XP_005262880.1:p.Ala341=
XM_006714137.3:c.1244C=	XP_006714200.1:p.Ala415=
XR_001741172.2:n.1763C=
NM_000128.4:c.1289C= MANE Select	NP_000119.1:p.Ala430=