Canonical Allele Identifier: CA1519936028

Gene: F11

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186280373G= , CM000666.2:g.186280373G=	GRCh38
NC_000004.11:g.187201527G= , CM000666.1:g.187201527G=	GRCh37
NC_000004.10:g.187438521G=	NCBI36
NG_008051.1:g.19410G= , LRG_583:g.19410G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1016G= MANE Select	ENSP00000384957.2:p.Cys339=
ENST00000264692.8:c.854G=	ENSP00000264692.5:p.Cys285=
ENST00000403665.6:c.1016G=	ENSP00000384957.2:p.Cys339=
ENST00000452239.1:c.463G=
NM_000128.3:c.1016G= , LRG_583t1:c.1016G=	NP_000119.1:p.Cys339=
XM_005262821.2:c.1016G=	XP_005262878.1:p.Cys339=
XM_005262822.2:c.1016G=	XP_005262879.1:p.Cys339=
XM_005262823.2:c.746G=	XP_005262880.1:p.Cys249=
XM_005262824.1:c.1016G=	XP_005262881.1:p.Cys339=
XM_006714137.1:c.968G=	XP_006714200.1:p.Cys323=
XR_938706.1:n.1368G=
XR_938707.1:n.1368G=
XM_005262821.4:c.1016G=	XP_005262878.1:p.Cys339=
XM_005262822.4:c.1016G=	XP_005262879.1:p.Cys339=
XM_005262823.4:c.746G=	XP_005262880.1:p.Cys249=
XM_006714137.3:c.968G=	XP_006714200.1:p.Cys323=
XM_017007884.2:c.1016G=	XP_016863373.1:p.Cys339=
XM_017007885.2:c.1016G=	XP_016863374.1:p.Cys339=
XM_017007886.2:c.1016G=	XP_016863375.1:p.Cys339=
XR_001741172.2:n.1349G=
NM_000128.4:c.1016G= MANE Select	NP_000119.1:p.Cys339=