Canonical Allele Identifier: CA1519936125

Gene: F11

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186280541A= , CM000666.2:g.186280541A=	GRCh38
NC_000004.11:g.187201695A= , CM000666.1:g.187201695A=	GRCh37
NC_000004.10:g.187438689A=	NCBI36
NG_008051.1:g.19578A= , LRG_583:g.19578A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1096A= MANE Select	ENSP00000384957.2:p.Ile366=
ENST00000264692.8:c.934A=	ENSP00000264692.5:p.Ile312=
ENST00000403665.6:c.1096A=	ENSP00000384957.2:p.Ile366=
ENST00000452239.1:c.543A=
NM_000128.3:c.1096A= , LRG_583t1:c.1096A=	NP_000119.1:p.Ile366=
XM_005262821.2:c.1099A=	XP_005262878.1:p.Ile367=
XM_005262822.2:c.1099A=	XP_005262879.1:p.Ile367=
XM_005262823.2:c.829A=	XP_005262880.1:p.Ile277=
XM_005262824.1:c.1099A=	XP_005262881.1:p.Ile367=
XM_006714137.1:c.1051A=	XP_006714200.1:p.Ile351=
XR_938706.1:n.1451A=
XR_938707.1:n.1451A=
XM_005262821.4:c.1099A=	XP_005262878.1:p.Ile367=
XM_005262822.4:c.1099A=	XP_005262879.1:p.Ile367=
XM_005262823.4:c.829A=	XP_005262880.1:p.Ile277=
XM_006714137.3:c.1051A=	XP_006714200.1:p.Ile351=
XM_017007884.2:c.1099A=	XP_016863373.1:p.Ile367=
XM_017007885.2:c.1099A=	XP_016863374.1:p.Ile367=
XM_017007886.2:c.1096A=	XP_016863375.1:p.Ile366=
XR_001741172.2:n.1517A=
NM_000128.4:c.1096A= MANE Select	NP_000119.1:p.Ile366=