Canonical Allele Identifier: CA1266824947

Gene: GGCX

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85551967C= , CM000664.2:g.85551967C=	GRCh38
NC_000002.11:g.85779090C= , CM000664.1:g.85779090C=	GRCh37
NC_000002.10:g.85632601C=	NCBI36
NG_011811.2:g.14568G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000473665.2:n.5932G=
ENST00000482662.2:n.4339G=
ENST00000685865.1:n.2291G=
ENST00000687250.1:n.1991G=
ENST00000687995.1:n.1806G=
ENST00000688205.1:c.*1047G=	ENSP00000509673.1:n.*1047G=
ENST00000688788.1:n.1693G=
ENST00000689276.1:c.1385G=	ENSP00000510012.1:p.Arg462=
ENST00000689576.1:c.*73G=	ENSP00000508712.1:n.*73G=
ENST00000690108.1:c.*1110G=	ENSP00000510617.1:n.*1110G=
ENST00000690468.1:c.*6G=	ENSP00000509078.1:n.*6G=
ENST00000690595.1:c.779G=	ENSP00000508979.1:p.Arg260=
ENST00000691348.1:c.*6G=	ENSP00000509369.1:n.*6G=
ENST00000691410.1:c.*1031G=	ENSP00000508479.1:n.*1031G=
ENST00000693287.1:c.770G=	ENSP00000510264.1:p.Arg257=
ENST00000693681.1:c.767G=	ENSP00000510789.1:p.Arg256=
ENST00000233838.9:c.1454G= MANE Select	ENSP00000233838.3:p.Arg485=
ENST00000233838.8:c.1454G=	ENSP00000233838.3:p.Arg485=
ENST00000430215.7:c.1283G=	ENSP00000408045.3:p.Arg428=
ENST00000465637.5:n.179-3963G=
NM_000821.5:c.1454G=	NP_000812.2:p.Arg485=
NM_000821.6:c.1454G=	NP_000812.2:p.Arg485=
NM_001142269.2:c.1283G=	NP_001135741.1:p.Arg428=
NM_001142269.3:c.1283G=	NP_001135741.1:p.Arg428=
XM_005264259.3:c.1454G=	XP_005264316.1:p.Arg485=
XM_011532764.1:c.632G=	XP_011531066.1:p.Arg211=
XM_011532765.1:c.632G=	XP_011531067.1:p.Arg211=
XR_939677.1:n.1367G=
XM_005264259.5:c.1454G=	XP_005264316.1:p.Arg485=
XM_011532764.3:c.632G=	XP_011531066.1:p.Arg211=
XM_011532765.3:c.632G=	XP_011531067.1:p.Arg211=
XM_017003803.2:c.1283G=	XP_016859292.1:p.Arg428=
XR_001738703.2:n.1367G=
NM_000821.7:c.1454G= MANE Select	NP_000812.2:p.Arg485=
NM_001142269.4:c.1283G=	NP_001135741.1:p.Arg428=