Canonical Allele Identifier: CA1519935995

Gene: F11

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186280304C= , CM000666.2:g.186280304C=	GRCh38
NC_000004.11:g.187201458C= , CM000666.1:g.187201458C=	GRCh37
NC_000004.10:g.187438452C=	NCBI36
NG_008051.1:g.19341C= , LRG_583:g.19341C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.947C= MANE Select	ENSP00000384957.2:p.Ala316=
ENST00000264692.8:c.785C=	ENSP00000264692.5:p.Ala262=
ENST00000403665.6:c.947C=	ENSP00000384957.2:p.Ala316=
ENST00000452239.1:c.394C=
NM_000128.3:c.947C= , LRG_583t1:c.947C=	NP_000119.1:p.Ala316=
XM_005262821.2:c.947C=	XP_005262878.1:p.Ala316=
XM_005262822.2:c.947C=	XP_005262879.1:p.Ala316=
XM_005262823.2:c.677C=	XP_005262880.1:p.Ala226=
XM_005262824.1:c.947C=	XP_005262881.1:p.Ala316=
XM_006714137.1:c.899C=	XP_006714200.1:p.Ala300=
XR_938706.1:n.1299C=
XR_938707.1:n.1299C=
XM_005262821.4:c.947C=	XP_005262878.1:p.Ala316=
XM_005262822.4:c.947C=	XP_005262879.1:p.Ala316=
XM_005262823.4:c.677C=	XP_005262880.1:p.Ala226=
XM_006714137.3:c.899C=	XP_006714200.1:p.Ala300=
XM_017007884.2:c.947C=	XP_016863373.1:p.Ala316=
XM_017007885.2:c.947C=	XP_016863374.1:p.Ala316=
XM_017007886.2:c.947C=	XP_016863375.1:p.Ala316=
XR_001741172.2:n.1280C=
NM_000128.4:c.947C= MANE Select	NP_000119.1:p.Ala316=