Canonical Allele Identifier: CA1519937789

Gene: F11

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186284191A= , CM000666.2:g.186284191A=	GRCh38
NC_000004.11:g.187205345A= , CM000666.1:g.187205345A=	GRCh37
NC_000004.10:g.187442339A=	NCBI36
NG_008051.1:g.23228A= , LRG_583:g.23228A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1235A= MANE Select	ENSP00000384957.2:p.Gln412=
ENST00000264692.8:c.1073A=	ENSP00000264692.5:p.Gln358=
ENST00000403665.6:c.1235A=	ENSP00000384957.2:p.Gln412=
NM_000128.3:c.1235A= , LRG_583t1:c.1235A=	NP_000119.1:p.Gln412=
XM_005262821.2:c.1238A=	XP_005262878.1:p.Gln413=
XM_005262822.2:c.1238A=	XP_005262879.1:p.Gln413=
XM_005262823.2:c.968A=	XP_005262880.1:p.Gln323=
XM_005262824.1:c.1238A=	XP_005262881.1:p.Gln413=
XM_006714137.1:c.1190A=	XP_006714200.1:p.Gln397=
XR_938706.1:n.1643A=
XR_938707.1:n.1643A=
XM_005262821.4:c.1238A=	XP_005262878.1:p.Gln413=
XM_005262822.4:c.1238A=	XP_005262879.1:p.Gln413=
XM_005262823.4:c.968A=	XP_005262880.1:p.Gln323=
XM_006714137.3:c.1190A=	XP_006714200.1:p.Gln397=
XR_001741172.2:n.1709A=
NM_000128.4:c.1235A= MANE Select	NP_000119.1:p.Gln412=