Canonical Allele Identifier: CA1519937754

Gene: F11

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186284139G= , CM000666.2:g.186284139G=	GRCh38
NC_000004.11:g.187205293G= , CM000666.1:g.187205293G=	GRCh37
NC_000004.10:g.187442287G=	NCBI36
NG_008051.1:g.23176G= , LRG_583:g.23176G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000403665.7:c.1183G= MANE Select	ENSP00000384957.2:p.Val395=
ENST00000264692.8:c.1021G=	ENSP00000264692.5:p.Val341=
ENST00000403665.6:c.1183G=	ENSP00000384957.2:p.Val395=
NM_000128.3:c.1183G= , LRG_583t1:c.1183G=	NP_000119.1:p.Val395=
XM_005262821.2:c.1186G=	XP_005262878.1:p.Val396=
XM_005262822.2:c.1186G=	XP_005262879.1:p.Val396=
XM_005262823.2:c.916G=	XP_005262880.1:p.Val306=
XM_005262824.1:c.1186G=	XP_005262881.1:p.Val396=
XM_006714137.1:c.1138G=	XP_006714200.1:p.Val380=
XR_938706.1:n.1591G=
XR_938707.1:n.1591G=
XM_005262821.4:c.1186G=	XP_005262878.1:p.Val396=
XM_005262822.4:c.1186G=	XP_005262879.1:p.Val396=
XM_005262823.4:c.916G=	XP_005262880.1:p.Val306=
XM_006714137.3:c.1138G=	XP_006714200.1:p.Val380=
XM_017007884.2:c.*2155G=	XP_016863373.1:n.*2155G=
XM_017007885.2:c.*51G=	XP_016863374.1:n.*51G=
XR_001741172.2:n.1657G=
NM_000128.4:c.1183G= MANE Select	NP_000119.1:p.Val395=