Canonical Allele Identifier: CA1266824934

Gene: GGCX

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85551940G= , CM000664.2:g.85551940G=	GRCh38
NC_000002.11:g.85779063G= , CM000664.1:g.85779063G=	GRCh37
NC_000002.10:g.85632574G=	NCBI36
NG_011811.2:g.14595C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000473665.2:n.5959C=
ENST00000482662.2:n.4366C=
ENST00000685865.1:n.2318C=
ENST00000687250.1:n.2018C=
ENST00000687995.1:n.1833C=
ENST00000688205.1:c.*1074C=	ENSP00000509673.1:n.*1074C=
ENST00000688788.1:n.1720C=
ENST00000689276.1:c.1412C=	ENSP00000510012.1:p.Ser471=
ENST00000689576.1:c.*100C=	ENSP00000508712.1:n.*100C=
ENST00000690108.1:c.*1137C=	ENSP00000510617.1:n.*1137C=
ENST00000690468.1:c.*33C=	ENSP00000509078.1:n.*33C=
ENST00000690595.1:c.806C=	ENSP00000508979.1:p.Ser269=
ENST00000691348.1:c.*33C=	ENSP00000509369.1:n.*33C=
ENST00000691410.1:c.*1058C=	ENSP00000508479.1:n.*1058C=
ENST00000693287.1:c.797C=	ENSP00000510264.1:p.Ser266=
ENST00000693681.1:c.794C=	ENSP00000510789.1:p.Ser265=
ENST00000233838.9:c.1481C= MANE Select	ENSP00000233838.3:p.Ser494=
ENST00000233838.8:c.1481C=	ENSP00000233838.3:p.Ser494=
ENST00000430215.7:c.1310C=	ENSP00000408045.3:p.Ser437=
ENST00000465637.5:n.179-3936C=
NM_000821.5:c.1481C=	NP_000812.2:p.Ser494=
NM_000821.6:c.1481C=	NP_000812.2:p.Ser494=
NM_001142269.2:c.1310C=	NP_001135741.1:p.Ser437=
NM_001142269.3:c.1310C=	NP_001135741.1:p.Ser437=
XM_005264259.3:c.1481C=	XP_005264316.1:p.Ser494=
XM_011532764.1:c.659C=	XP_011531066.1:p.Ser220=
XM_011532765.1:c.659C=	XP_011531067.1:p.Ser220=
XR_939677.1:n.1394C=
XM_005264259.5:c.1481C=	XP_005264316.1:p.Ser494=
XM_011532764.3:c.659C=	XP_011531066.1:p.Ser220=
XM_011532765.3:c.659C=	XP_011531067.1:p.Ser220=
XM_017003803.2:c.1310C=	XP_016859292.1:p.Ser437=
XR_001738703.2:n.1394C=
NM_000821.7:c.1481C= MANE Select	NP_000812.2:p.Ser494=
NM_001142269.4:c.1310C=	NP_001135741.1:p.Ser437=