Canonical Allele Identifier: CA1519933265

Gene: F11

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186274219C= , CM000666.2:g.186274219C=	GRCh38
NC_000004.11:g.187195373C= , CM000666.1:g.187195373C=	GRCh37
NC_000004.10:g.187432367C=	NCBI36
NG_008051.1:g.13256C= , LRG_583:g.13256C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.429C= MANE Select	ENSP00000384957.2:p.Asp143=
ENST00000264692.8:c.323+1044C=	ENSP00000264692.5:n.323+1044C=
ENST00000403665.6:c.429C=	ENSP00000384957.2:p.Asp143=
ENST00000492972.6:c.429C=	ENSP00000424479.1:p.Asp143=
ENST00000514715.1:n.301C=
NM_000128.3:c.429C= , LRG_583t1:c.429C=	NP_000119.1:p.Asp143=
XM_005262821.2:c.429C=	XP_005262878.1:p.Asp143=
XM_005262822.2:c.429C=	XP_005262879.1:p.Asp143=
XM_005262823.2:c.429C=	XP_005262880.1:p.Asp143=
XM_005262824.1:c.429C=	XP_005262881.1:p.Asp143=
XM_006714137.1:c.429C=	XP_006714200.1:p.Asp143=
XR_938706.1:n.781C=
XR_938707.1:n.781C=
NM_001354804.1:c.429C=	NP_001341733.1:p.Asp143=
XM_005262821.4:c.429C=	XP_005262878.1:p.Asp143=
XM_005262822.4:c.429C=	XP_005262879.1:p.Asp143=
XM_005262823.4:c.429C=	XP_005262880.1:p.Asp143=
XM_006714137.3:c.429C=	XP_006714200.1:p.Asp143=
XM_017007884.2:c.429C=	XP_016863373.1:p.Asp143=
XM_017007885.2:c.429C=	XP_016863374.1:p.Asp143=
XM_017007886.2:c.429C=	XP_016863375.1:p.Asp143=
XR_001741172.2:n.762C=
NM_000128.4:c.429C= MANE Select	NP_000119.1:p.Asp143=
NM_001354804.2:c.429C=	NP_001341733.1:p.Asp143=