Canonical Allele Identifier: CA1266825394

Gene: GGCX

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85553009C= , CM000664.2:g.85553009C=	GRCh38
NC_000002.11:g.85780132C= , CM000664.1:g.85780132C=	GRCh37
NC_000002.10:g.85633643C=	NCBI36
NG_011811.2:g.13526G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000473665.2:n.5261G=
ENST00000482662.2:n.3668G=
ENST00000685865.1:n.1620G=
ENST00000687250.1:n.1320G=
ENST00000687995.1:n.1569G=
ENST00000688205.1:c.*810G=	ENSP00000509673.1:n.*810G=
ENST00000688788.1:n.1456G=
ENST00000689276.1:c.1148G=	ENSP00000510012.1:p.Arg383=
ENST00000689576.1:c.1217G=	ENSP00000508712.1:p.Arg406=
ENST00000690108.1:c.*873G=	ENSP00000510617.1:n.*873G=
ENST00000690468.1:c.938G=	ENSP00000509078.1:p.Arg313=
ENST00000690595.1:c.542G=	ENSP00000508979.1:p.Arg181=
ENST00000691348.1:c.1046G=	ENSP00000509369.1:p.Arg349=
ENST00000691410.1:c.*794G=	ENSP00000508479.1:n.*794G=
ENST00000693287.1:c.533G=	ENSP00000510264.1:p.Arg178=
ENST00000693681.1:c.530G=	ENSP00000510789.1:p.Arg177=
ENST00000233838.9:c.1217G= MANE Select	ENSP00000233838.3:p.Arg406=
ENST00000233838.8:c.1217G=	ENSP00000233838.3:p.Arg406=
ENST00000430215.7:c.1046G=	ENSP00000408045.3:p.Arg349=
ENST00000465637.5:n.179-5005G=
ENST00000473665.1:n.710G=
ENST00000482662.1:n.634G=
NM_000821.5:c.1217G=	NP_000812.2:p.Arg406=
NM_000821.6:c.1217G=	NP_000812.2:p.Arg406=
NM_001142269.2:c.1046G=	NP_001135741.1:p.Arg349=
NM_001142269.3:c.1046G=	NP_001135741.1:p.Arg349=
XM_005264259.3:c.1217G=	XP_005264316.1:p.Arg406=
XM_011532764.1:c.395G=	XP_011531066.1:p.Arg132=
XM_011532765.1:c.395G=	XP_011531067.1:p.Arg132=
XR_939677.1:n.1282G=
XM_005264259.5:c.1217G=	XP_005264316.1:p.Arg406=
XM_011532764.3:c.395G=	XP_011531066.1:p.Arg132=
XM_011532765.3:c.395G=	XP_011531067.1:p.Arg132=
XM_017003803.2:c.1046G=	XP_016859292.1:p.Arg349=
XR_001738703.2:n.1282G=
NM_000821.7:c.1217G= MANE Select	NP_000812.2:p.Arg406=
NM_001142269.4:c.1046G=	NP_001135741.1:p.Arg349=