Canonical Allele Identifier: CA1519937762

Gene: F11

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186284150G= , CM000666.2:g.186284150G=	GRCh38
NC_000004.11:g.187205304G= , CM000666.1:g.187205304G=	GRCh37
NC_000004.10:g.187442298G=	NCBI36
NG_008051.1:g.23187G= , LRG_583:g.23187G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000403665.7:c.1194G= MANE Select	ENSP00000384957.2:p.Glu398=
ENST00000264692.8:c.1032G=	ENSP00000264692.5:p.Glu344=
ENST00000403665.6:c.1194G=	ENSP00000384957.2:p.Glu398=
NM_000128.3:c.1194G= , LRG_583t1:c.1194G=	NP_000119.1:p.Glu398=
XM_005262821.2:c.1197G=	XP_005262878.1:p.Glu399=
XM_005262822.2:c.1197G=	XP_005262879.1:p.Glu399=
XM_005262823.2:c.927G=	XP_005262880.1:p.Glu309=
XM_005262824.1:c.1197G=	XP_005262881.1:p.Glu399=
XM_006714137.1:c.1149G=	XP_006714200.1:p.Glu383=
XR_938706.1:n.1602G=
XR_938707.1:n.1602G=
XM_005262821.4:c.1197G=	XP_005262878.1:p.Glu399=
XM_005262822.4:c.1197G=	XP_005262879.1:p.Glu399=
XM_005262823.4:c.927G=	XP_005262880.1:p.Glu309=
XM_006714137.3:c.1149G=	XP_006714200.1:p.Glu383=
XM_017007884.2:c.*2166G=	XP_016863373.1:n.*2166G=
XM_017007885.2:c.*62G=	XP_016863374.1:n.*62G=
XR_001741172.2:n.1668G=
NM_000128.4:c.1194G= MANE Select	NP_000119.1:p.Glu398=