Canonical Allele Identifier: CA347487404

Gene: GGCX

Linked Data

• MyVariant Identifiers: chr2:g.85780389T>C (hg19) ; chr2:g.85553266T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85553266T>C , CM000664.2:g.85553266T>C	GRCh38
NC_000002.11:g.85780389T>C , CM000664.1:g.85780389T>C	GRCh37
NC_000002.10:g.85633900T>C	NCBI36
NG_011811.2:g.13269A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000473665.2:n.5165A>G
ENST00000482662.2:n.3572A>G
ENST00000685865.1:n.1524A>G
ENST00000687250.1:n.1224A>G
ENST00000687995.1:n.1473A>G
ENST00000688205.1:c.*714A>G	ENSP00000509673.1:n.*714A>G
ENST00000688788.1:n.1360A>G
ENST00000689276.1:c.1052A>G	ENSP00000510012.1:p.Gln351Arg
ENST00000689576.1:c.1121A>G	ENSP00000508712.1:p.Gln374Arg
ENST00000690108.1:c.*777A>G	ENSP00000510617.1:n.*777A>G
ENST00000690468.1:c.842A>G	ENSP00000509078.1:p.Gln281Arg
ENST00000690595.1:c.446A>G	ENSP00000508979.1:p.Gln149Arg
ENST00000691348.1:c.950A>G	ENSP00000509369.1:p.Gln317Arg
ENST00000691410.1:c.*698A>G	ENSP00000508479.1:n.*698A>G
ENST00000693287.1:c.437A>G	ENSP00000510264.1:p.Gln146Arg
ENST00000693681.1:c.434A>G	ENSP00000510789.1:p.Gln145Arg
ENST00000233838.9:c.1121A>G MANE Select	ENSP00000233838.3:p.Gln374Arg
ENST00000233838.8:c.1121A>G	ENSP00000233838.3:p.Gln374Arg
ENST00000430215.7:c.950A>G	ENSP00000408045.3:p.Gln317Arg
ENST00000465637.5:n.179-5262A>G
ENST00000473665.1:n.614A>G
ENST00000482662.1:n.538A>G
NM_000821.5:c.1121A>G	NP_000812.2:p.Gln374Arg
NM_000821.6:c.1121A>G	NP_000812.2:p.Gln374Arg
NM_001142269.2:c.950A>G	NP_001135741.1:p.Gln317Arg
NM_001142269.3:c.950A>G	NP_001135741.1:p.Gln317Arg
XM_005264259.3:c.1121A>G	XP_005264316.1:p.Gln374Arg
XM_011532764.1:c.299A>G	XP_011531066.1:p.Gln100Arg
XM_011532765.1:c.299A>G	XP_011531067.1:p.Gln100Arg
XR_939677.1:n.1186A>G
XM_005264259.5:c.1121A>G	XP_005264316.1:p.Gln374Arg
XM_011532764.3:c.299A>G	XP_011531066.1:p.Gln100Arg
XM_011532765.3:c.299A>G	XP_011531067.1:p.Gln100Arg
XM_017003803.2:c.950A>G	XP_016859292.1:p.Gln317Arg
XR_001738703.2:n.1186A>G
NM_000821.7:c.1121A>G MANE Select	NP_000812.2:p.Gln374Arg
NM_001142269.4:c.950A>G	NP_001135741.1:p.Gln317Arg