Canonical Allele Identifier: CA347487136

Gene: GGCX

Linked Data

• dbSNP Id: rs1692037713
• MyVariant Identifiers: chr2:g.85780172C>T (hg19) ; chr2:g.85553049C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85553049C>T , CM000664.2:g.85553049C>T	GRCh38
NC_000002.11:g.85780172C>T , CM000664.1:g.85780172C>T	GRCh37
NC_000002.10:g.85633683C>T	NCBI36
NG_011811.2:g.13486G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000473665.2:n.5221G>A
ENST00000482662.2:n.3628G>A
ENST00000685865.1:n.1580G>A
ENST00000687250.1:n.1280G>A
ENST00000687995.1:n.1529G>A
ENST00000688205.1:c.*770G>A	ENSP00000509673.1:n.*770G>A
ENST00000688788.1:n.1416G>A
ENST00000689276.1:c.1108G>A	ENSP00000510012.1:p.Gly370Arg
ENST00000689576.1:c.1177G>A	ENSP00000508712.1:p.Gly393Arg
ENST00000690108.1:c.*833G>A	ENSP00000510617.1:n.*833G>A
ENST00000690468.1:c.898G>A	ENSP00000509078.1:p.Gly300Arg
ENST00000690595.1:c.502G>A	ENSP00000508979.1:p.Gly168Arg
ENST00000691348.1:c.1006G>A	ENSP00000509369.1:p.Gly336Arg
ENST00000691410.1:c.*754G>A	ENSP00000508479.1:n.*754G>A
ENST00000693287.1:c.493G>A	ENSP00000510264.1:p.Gly165Arg
ENST00000693681.1:c.490G>A	ENSP00000510789.1:p.Gly164Arg
ENST00000233838.9:c.1177G>A MANE Select	ENSP00000233838.3:p.Gly393Arg
ENST00000233838.8:c.1177G>A	ENSP00000233838.3:p.Gly393Arg
ENST00000430215.7:c.1006G>A	ENSP00000408045.3:p.Gly336Arg
ENST00000465637.5:n.179-5045G>A
ENST00000473665.1:n.670G>A
ENST00000482662.1:n.594G>A
NM_000821.5:c.1177G>A	NP_000812.2:p.Gly393Arg
NM_000821.6:c.1177G>A	NP_000812.2:p.Gly393Arg
NM_001142269.2:c.1006G>A	NP_001135741.1:p.Gly336Arg
NM_001142269.3:c.1006G>A	NP_001135741.1:p.Gly336Arg
XM_005264259.3:c.1177G>A	XP_005264316.1:p.Gly393Arg
XM_011532764.1:c.355G>A	XP_011531066.1:p.Gly119Arg
XM_011532765.1:c.355G>A	XP_011531067.1:p.Gly119Arg
XR_939677.1:n.1242G>A
XM_005264259.5:c.1177G>A	XP_005264316.1:p.Gly393Arg
XM_011532764.3:c.355G>A	XP_011531066.1:p.Gly119Arg
XM_011532765.3:c.355G>A	XP_011531067.1:p.Gly119Arg
XM_017003803.2:c.1006G>A	XP_016859292.1:p.Gly336Arg
XR_001738703.2:n.1242G>A
NM_000821.7:c.1177G>A MANE Select	NP_000812.2:p.Gly393Arg
NM_001142269.4:c.1006G>A	NP_001135741.1:p.Gly336Arg