Canonical Allele Identifier: CA347486856

Gene: GGCX

Linked Data

• MyVariant Identifiers: chr2:g.85780096C>G (hg19) ; chr2:g.85552973C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85552973C>G , CM000664.2:g.85552973C>G	GRCh38
NC_000002.11:g.85780096C>G , CM000664.1:g.85780096C>G	GRCh37
NC_000002.10:g.85633607C>G	NCBI36
NG_011811.2:g.13562G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000473665.2:n.5297G>C
ENST00000482662.2:n.3704G>C
ENST00000685865.1:n.1656G>C
ENST00000687250.1:n.1356G>C
ENST00000687995.1:n.1605G>C
ENST00000688205.1:c.*846G>C	ENSP00000509673.1:n.*846G>C
ENST00000688788.1:n.1492G>C
ENST00000689276.1:c.1184G>C	ENSP00000510012.1:p.Gly395Ala
ENST00000689576.1:c.1253G>C	ENSP00000508712.1:p.Gly418Ala
ENST00000690108.1:c.*909G>C	ENSP00000510617.1:n.*909G>C
ENST00000690468.1:c.974G>C	ENSP00000509078.1:p.Gly325Ala
ENST00000690595.1:c.578G>C	ENSP00000508979.1:p.Gly193Ala
ENST00000691348.1:c.1082G>C	ENSP00000509369.1:p.Gly361Ala
ENST00000691410.1:c.*830G>C	ENSP00000508479.1:n.*830G>C
ENST00000693287.1:c.569G>C	ENSP00000510264.1:p.Gly190Ala
ENST00000693681.1:c.566G>C	ENSP00000510789.1:p.Gly189Ala
ENST00000233838.9:c.1253G>C MANE Select	ENSP00000233838.3:p.Gly418Ala
ENST00000233838.8:c.1253G>C	ENSP00000233838.3:p.Gly418Ala
ENST00000430215.7:c.1082G>C	ENSP00000408045.3:p.Gly361Ala
ENST00000465637.5:n.179-4969G>C
ENST00000473665.1:n.746G>C
ENST00000482662.1:n.670G>C
NM_000821.5:c.1253G>C	NP_000812.2:p.Gly418Ala
NM_000821.6:c.1253G>C	NP_000812.2:p.Gly418Ala
NM_001142269.2:c.1082G>C	NP_001135741.1:p.Gly361Ala
NM_001142269.3:c.1082G>C	NP_001135741.1:p.Gly361Ala
XM_005264259.3:c.1253G>C	XP_005264316.1:p.Gly418Ala
XM_011532764.1:c.431G>C	XP_011531066.1:p.Gly144Ala
XM_011532765.1:c.431G>C	XP_011531067.1:p.Gly144Ala
XR_939677.1:n.1318G>C
XM_005264259.5:c.1253G>C	XP_005264316.1:p.Gly418Ala
XM_011532764.3:c.431G>C	XP_011531066.1:p.Gly144Ala
XM_011532765.3:c.431G>C	XP_011531067.1:p.Gly144Ala
XM_017003803.2:c.1082G>C	XP_016859292.1:p.Gly361Ala
XR_001738703.2:n.1318G>C
NM_000821.7:c.1253G>C MANE Select	NP_000812.2:p.Gly418Ala
NM_001142269.4:c.1082G>C	NP_001135741.1:p.Gly361Ala