Canonical Allele Identifier: CA1519934219

Gene: F11

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186276365C= , CM000666.2:g.186276365C=	GRCh38
NC_000004.11:g.187197519C= , CM000666.1:g.187197519C=	GRCh37
NC_000004.10:g.187434513C=	NCBI36
NG_008051.1:g.15402C= , LRG_583:g.15402C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.730C= MANE Select	ENSP00000384957.2:p.Gln244=
ENST00000264692.8:c.568C=	ENSP00000264692.5:p.Gln190=
ENST00000403665.6:c.730C=	ENSP00000384957.2:p.Gln244=
ENST00000452239.1:c.177C=
NM_000128.3:c.730C= , LRG_583t1:c.730C=	NP_000119.1:p.Gln244=
XM_005262821.2:c.730C=	XP_005262878.1:p.Gln244=
XM_005262822.2:c.730C=	XP_005262879.1:p.Gln244=
XM_005262823.2:c.485+2090C=	XP_005262880.1:n.485+2090C=
XM_005262824.1:c.730C=	XP_005262881.1:p.Gln244=
XM_006714137.1:c.730C=	XP_006714200.1:p.Gln244=
XR_938706.1:n.1082C=
XR_938707.1:n.1082C=
XM_005262821.4:c.730C=	XP_005262878.1:p.Gln244=
XM_005262822.4:c.730C=	XP_005262879.1:p.Gln244=
XM_005262823.4:c.485+2090C=	XP_005262880.1:n.485+2090C=
XM_006714137.3:c.730C=	XP_006714200.1:p.Gln244=
XM_017007884.2:c.730C=	XP_016863373.1:p.Gln244=
XM_017007885.2:c.730C=	XP_016863374.1:p.Gln244=
XM_017007886.2:c.730C=	XP_016863375.1:p.Gln244=
XR_001741172.2:n.1063C=
NM_000128.4:c.730C= MANE Select	NP_000119.1:p.Gln244=