Canonical Allele Identifier: CA1519937751

Gene: F11

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186284134C= , CM000666.2:g.186284134C=	GRCh38
NC_000004.11:g.187205288C= , CM000666.1:g.187205288C=	GRCh37
NC_000004.10:g.187442282C=	NCBI36
NG_008051.1:g.23171C= , LRG_583:g.23171C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1178C= MANE Select	ENSP00000384957.2:p.Ala393=
ENST00000264692.8:c.1016C=	ENSP00000264692.5:p.Ala339=
ENST00000403665.6:c.1178C=	ENSP00000384957.2:p.Ala393=
NM_000128.3:c.1178C= , LRG_583t1:c.1178C=	NP_000119.1:p.Ala393=
XM_005262821.2:c.1181C=	XP_005262878.1:p.Ala394=
XM_005262822.2:c.1181C=	XP_005262879.1:p.Ala394=
XM_005262823.2:c.911C=	XP_005262880.1:p.Ala304=
XM_005262824.1:c.1181C=	XP_005262881.1:p.Ala394=
XM_006714137.1:c.1133C=	XP_006714200.1:p.Ala378=
XR_938706.1:n.1586C=
XR_938707.1:n.1586C=
XM_005262821.4:c.1181C=	XP_005262878.1:p.Ala394=
XM_005262822.4:c.1181C=	XP_005262879.1:p.Ala394=
XM_005262823.4:c.911C=	XP_005262880.1:p.Ala304=
XM_006714137.3:c.1133C=	XP_006714200.1:p.Ala378=
XM_017007884.2:c.*2150C=	XP_016863373.1:n.*2150C=
XM_017007885.2:c.*46C=	XP_016863374.1:n.*46C=
XR_001741172.2:n.1652C=
NM_000128.4:c.1178C= MANE Select	NP_000119.1:p.Ala393=