Canonical Allele Identifier: CA1519934174

Gene: F11

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186276277C= , CM000666.2:g.186276277C=	GRCh38
NC_000004.11:g.187197431C= , CM000666.1:g.187197431C=	GRCh37
NC_000004.10:g.187434425C=	NCBI36
NG_008051.1:g.15314C= , LRG_583:g.15314C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000403665.7:c.642C= MANE Select	ENSP00000384957.2:p.Asn214=
ENST00000264692.8:c.480C=	ENSP00000264692.5:p.Asn160=
ENST00000403665.6:c.642C=	ENSP00000384957.2:p.Asn214=
ENST00000452239.1:c.89C=
NM_000128.3:c.642C= , LRG_583t1:c.642C=	NP_000119.1:p.Asn214=
XM_005262821.2:c.642C=	XP_005262878.1:p.Asn214=
XM_005262822.2:c.642C=	XP_005262879.1:p.Asn214=
XM_005262823.2:c.485+2002C=	XP_005262880.1:n.485+2002C=
XM_005262824.1:c.642C=	XP_005262881.1:p.Asn214=
XM_006714137.1:c.642C=	XP_006714200.1:p.Asn214=
XR_938706.1:n.994C=
XR_938707.1:n.994C=
XM_005262821.4:c.642C=	XP_005262878.1:p.Asn214=
XM_005262822.4:c.642C=	XP_005262879.1:p.Asn214=
XM_005262823.4:c.485+2002C=	XP_005262880.1:n.485+2002C=
XM_006714137.3:c.642C=	XP_006714200.1:p.Asn214=
XM_017007884.2:c.642C=	XP_016863373.1:p.Asn214=
XM_017007885.2:c.642C=	XP_016863374.1:p.Asn214=
XM_017007886.2:c.642C=	XP_016863375.1:p.Asn214=
XR_001741172.2:n.975C=
NM_000128.4:c.642C= MANE Select	NP_000119.1:p.Asn214=