Canonical Allele Identifier: CA1266824944

Gene: GGCX

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85551956C= , CM000664.2:g.85551956C=	GRCh38
NC_000002.11:g.85779079C= , CM000664.1:g.85779079C=	GRCh37
NC_000002.10:g.85632590C=	NCBI36
NG_011811.2:g.14579G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000473665.2:n.5943G=
ENST00000482662.2:n.4350G=
ENST00000685865.1:n.2302G=
ENST00000687250.1:n.2002G=
ENST00000687995.1:n.1817G=
ENST00000688205.1:c.*1058G=	ENSP00000509673.1:n.*1058G=
ENST00000688788.1:n.1704G=
ENST00000689276.1:c.1396G=	ENSP00000510012.1:p.Val466=
ENST00000689576.1:c.*84G=	ENSP00000508712.1:n.*84G=
ENST00000690108.1:c.*1121G=	ENSP00000510617.1:n.*1121G=
ENST00000690468.1:c.*17G=	ENSP00000509078.1:n.*17G=
ENST00000690595.1:c.790G=	ENSP00000508979.1:p.Val264=
ENST00000691348.1:c.*17G=	ENSP00000509369.1:n.*17G=
ENST00000691410.1:c.*1042G=	ENSP00000508479.1:n.*1042G=
ENST00000693287.1:c.781G=	ENSP00000510264.1:p.Val261=
ENST00000693681.1:c.778G=	ENSP00000510789.1:p.Val260=
ENST00000233838.9:c.1465G= MANE Select	ENSP00000233838.3:p.Val489=
ENST00000233838.8:c.1465G=	ENSP00000233838.3:p.Val489=
ENST00000430215.7:c.1294G=	ENSP00000408045.3:p.Val432=
ENST00000465637.5:n.179-3952G=
NM_000821.5:c.1465G=	NP_000812.2:p.Val489=
NM_000821.6:c.1465G=	NP_000812.2:p.Val489=
NM_001142269.2:c.1294G=	NP_001135741.1:p.Val432=
NM_001142269.3:c.1294G=	NP_001135741.1:p.Val432=
XM_005264259.3:c.1465G=	XP_005264316.1:p.Val489=
XM_011532764.1:c.643G=	XP_011531066.1:p.Val215=
XM_011532765.1:c.643G=	XP_011531067.1:p.Val215=
XR_939677.1:n.1378G=
XM_005264259.5:c.1465G=	XP_005264316.1:p.Val489=
XM_011532764.3:c.643G=	XP_011531066.1:p.Val215=
XM_011532765.3:c.643G=	XP_011531067.1:p.Val215=
XM_017003803.2:c.1294G=	XP_016859292.1:p.Val432=
XR_001738703.2:n.1378G=
NM_000821.7:c.1465G= MANE Select	NP_000812.2:p.Val489=
NM_001142269.4:c.1294G=	NP_001135741.1:p.Val432=