Canonical Allele Identifier: CA1519937745

Gene: F11

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186284120C= , CM000666.2:g.186284120C=	GRCh38
NC_000004.11:g.187205274C= , CM000666.1:g.187205274C=	GRCh37
NC_000004.10:g.187442268C=	NCBI36
NG_008051.1:g.23157C= , LRG_583:g.23157C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1164C= MANE Select	ENSP00000384957.2:p.Ile388=
ENST00000264692.8:c.1002C=	ENSP00000264692.5:p.Ile334=
ENST00000403665.6:c.1164C=	ENSP00000384957.2:p.Ile388=
NM_000128.3:c.1164C= , LRG_583t1:c.1164C=	NP_000119.1:p.Ile388=
XM_005262821.2:c.1167C=	XP_005262878.1:p.Ile389=
XM_005262822.2:c.1167C=	XP_005262879.1:p.Ile389=
XM_005262823.2:c.897C=	XP_005262880.1:p.Ile299=
XM_005262824.1:c.1167C=	XP_005262881.1:p.Ile389=
XM_006714137.1:c.1119C=	XP_006714200.1:p.Ile373=
XR_938706.1:n.1572C=
XR_938707.1:n.1572C=
XM_005262821.4:c.1167C=	XP_005262878.1:p.Ile389=
XM_005262822.4:c.1167C=	XP_005262879.1:p.Ile389=
XM_005262823.4:c.897C=	XP_005262880.1:p.Ile299=
XM_006714137.3:c.1119C=	XP_006714200.1:p.Ile373=
XM_017007884.2:c.*2136C=	XP_016863373.1:n.*2136C=
XM_017007885.2:c.*32C=	XP_016863374.1:n.*32C=
XR_001741172.2:n.1638C=
NM_000128.4:c.1164C= MANE Select	NP_000119.1:p.Ile388=