Canonical Allele Identifier: CA1519937760

Gene: F11

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186284147T= , CM000666.2:g.186284147T=	GRCh38
NC_000004.11:g.187205301T= , CM000666.1:g.187205301T=	GRCh37
NC_000004.10:g.187442295T=	NCBI36
NG_008051.1:g.23184T= , LRG_583:g.23184T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1191T= MANE Select	ENSP00000384957.2:p.Gly397=
ENST00000264692.8:c.1029T=	ENSP00000264692.5:p.Gly343=
ENST00000403665.6:c.1191T=	ENSP00000384957.2:p.Gly397=
NM_000128.3:c.1191T= , LRG_583t1:c.1191T=	NP_000119.1:p.Gly397=
XM_005262821.2:c.1194T=	XP_005262878.1:p.Gly398=
XM_005262822.2:c.1194T=	XP_005262879.1:p.Gly398=
XM_005262823.2:c.924T=	XP_005262880.1:p.Gly308=
XM_005262824.1:c.1194T=	XP_005262881.1:p.Gly398=
XM_006714137.1:c.1146T=	XP_006714200.1:p.Gly382=
XR_938706.1:n.1599T=
XR_938707.1:n.1599T=
XM_005262821.4:c.1194T=	XP_005262878.1:p.Gly398=
XM_005262822.4:c.1194T=	XP_005262879.1:p.Gly398=
XM_005262823.4:c.924T=	XP_005262880.1:p.Gly308=
XM_006714137.3:c.1146T=	XP_006714200.1:p.Gly382=
XM_017007884.2:c.*2163T=	XP_016863373.1:n.*2163T=
XM_017007885.2:c.*59T=	XP_016863374.1:n.*59T=
XR_001741172.2:n.1665T=
NM_000128.4:c.1191T= MANE Select	NP_000119.1:p.Gly397=