Canonical Allele Identifier: CA1266825368

Gene: GGCX

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85552970C= , CM000664.2:g.85552970C=	GRCh38
NC_000002.11:g.85780093C= , CM000664.1:g.85780093C=	GRCh37
NC_000002.10:g.85633604C=	NCBI36
NG_011811.2:g.13565G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000473665.2:n.5300G=
ENST00000482662.2:n.3707G=
ENST00000685865.1:n.1659G=
ENST00000687250.1:n.1359G=
ENST00000687995.1:n.1608G=
ENST00000688205.1:c.*849G=	ENSP00000509673.1:n.*849G=
ENST00000688788.1:n.1495G=
ENST00000689276.1:c.1187G=	ENSP00000510012.1:p.Arg396=
ENST00000689576.1:c.1256G=	ENSP00000508712.1:p.Arg419=
ENST00000690108.1:c.*912G=	ENSP00000510617.1:n.*912G=
ENST00000690468.1:c.977G=	ENSP00000509078.1:p.Arg326=
ENST00000690595.1:c.581G=	ENSP00000508979.1:p.Arg194=
ENST00000691348.1:c.1085G=	ENSP00000509369.1:p.Arg362=
ENST00000691410.1:c.*833G=	ENSP00000508479.1:n.*833G=
ENST00000693287.1:c.572G=	ENSP00000510264.1:p.Arg191=
ENST00000693681.1:c.569G=	ENSP00000510789.1:p.Arg190=
ENST00000233838.9:c.1256G= MANE Select	ENSP00000233838.3:p.Arg419=
ENST00000233838.8:c.1256G=	ENSP00000233838.3:p.Arg419=
ENST00000430215.7:c.1085G=	ENSP00000408045.3:p.Arg362=
ENST00000465637.5:n.179-4966G=
ENST00000473665.1:n.749G=
ENST00000482662.1:n.673G=
NM_000821.5:c.1256G=	NP_000812.2:p.Arg419=
NM_000821.6:c.1256G=	NP_000812.2:p.Arg419=
NM_001142269.2:c.1085G=	NP_001135741.1:p.Arg362=
NM_001142269.3:c.1085G=	NP_001135741.1:p.Arg362=
XM_005264259.3:c.1256G=	XP_005264316.1:p.Arg419=
XM_011532764.1:c.434G=	XP_011531066.1:p.Arg145=
XM_011532765.1:c.434G=	XP_011531067.1:p.Arg145=
XR_939677.1:n.1321G=
XM_005264259.5:c.1256G=	XP_005264316.1:p.Arg419=
XM_011532764.3:c.434G=	XP_011531066.1:p.Arg145=
XM_011532765.3:c.434G=	XP_011531067.1:p.Arg145=
XM_017003803.2:c.1085G=	XP_016859292.1:p.Arg362=
XR_001738703.2:n.1321G=
NM_000821.7:c.1256G= MANE Select	NP_000812.2:p.Arg419=
NM_001142269.4:c.1085G=	NP_001135741.1:p.Arg362=