Canonical Allele Identifier: CA1519937738

Gene: F11

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186284101C= , CM000666.2:g.186284101C=	GRCh38
NC_000004.11:g.187205255C= , CM000666.1:g.187205255C=	GRCh37
NC_000004.10:g.187442249C=	NCBI36
NG_008051.1:g.23138C= , LRG_583:g.23138C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000403665.7:c.1145C= MANE Select	ENSP00000384957.2:p.Thr382=
ENST00000264692.8:c.983C=	ENSP00000264692.5:p.Thr328=
ENST00000403665.6:c.1145C=	ENSP00000384957.2:p.Thr382=
NM_000128.3:c.1145C= , LRG_583t1:c.1145C=	NP_000119.1:p.Thr382=
XM_005262821.2:c.1148C=	XP_005262878.1:p.Thr383=
XM_005262822.2:c.1148C=	XP_005262879.1:p.Thr383=
XM_005262823.2:c.878C=	XP_005262880.1:p.Thr293=
XM_005262824.1:c.1148C=	XP_005262881.1:p.Thr383=
XM_006714137.1:c.1100C=	XP_006714200.1:p.Thr367=
XR_938706.1:n.1553C=
XR_938707.1:n.1553C=
XM_005262821.4:c.1148C=	XP_005262878.1:p.Thr383=
XM_005262822.4:c.1148C=	XP_005262879.1:p.Thr383=
XM_005262823.4:c.878C=	XP_005262880.1:p.Thr293=
XM_006714137.3:c.1100C=	XP_006714200.1:p.Thr367=
XM_017007884.2:c.*2117C=	XP_016863373.1:n.*2117C=
XM_017007885.2:c.*13C=	XP_016863374.1:n.*13C=
XR_001741172.2:n.1619C=
NM_000128.4:c.1145C= MANE Select	NP_000119.1:p.Thr382=