Canonical Allele Identifier: CA347486862

Gene: GGCX

Linked Data

• MyVariant Identifiers: chr2:g.85780099T>C (hg19) ; chr2:g.85552976T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85552976T>C , CM000664.2:g.85552976T>C	GRCh38
NC_000002.11:g.85780099T>C , CM000664.1:g.85780099T>C	GRCh37
NC_000002.10:g.85633610T>C	NCBI36
NG_011811.2:g.13559A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000473665.2:n.5294A>G
ENST00000482662.2:n.3701A>G
ENST00000685865.1:n.1653A>G
ENST00000687250.1:n.1353A>G
ENST00000687995.1:n.1602A>G
ENST00000688205.1:c.*843A>G	ENSP00000509673.1:n.*843A>G
ENST00000688788.1:n.1489A>G
ENST00000689276.1:c.1181A>G	ENSP00000510012.1:p.Asp394Gly
ENST00000689576.1:c.1250A>G	ENSP00000508712.1:p.Asp417Gly
ENST00000690108.1:c.*906A>G	ENSP00000510617.1:n.*906A>G
ENST00000690468.1:c.971A>G	ENSP00000509078.1:p.Asp324Gly
ENST00000690595.1:c.575A>G	ENSP00000508979.1:p.Asp192Gly
ENST00000691348.1:c.1079A>G	ENSP00000509369.1:p.Asp360Gly
ENST00000691410.1:c.*827A>G	ENSP00000508479.1:n.*827A>G
ENST00000693287.1:c.566A>G	ENSP00000510264.1:p.Asp189Gly
ENST00000693681.1:c.563A>G	ENSP00000510789.1:p.Asp188Gly
ENST00000233838.9:c.1250A>G MANE Select	ENSP00000233838.3:p.Asp417Gly
ENST00000233838.8:c.1250A>G	ENSP00000233838.3:p.Asp417Gly
ENST00000430215.7:c.1079A>G	ENSP00000408045.3:p.Asp360Gly
ENST00000465637.5:n.179-4972A>G
ENST00000473665.1:n.743A>G
ENST00000482662.1:n.667A>G
NM_000821.5:c.1250A>G	NP_000812.2:p.Asp417Gly
NM_000821.6:c.1250A>G	NP_000812.2:p.Asp417Gly
NM_001142269.2:c.1079A>G	NP_001135741.1:p.Asp360Gly
NM_001142269.3:c.1079A>G	NP_001135741.1:p.Asp360Gly
XM_005264259.3:c.1250A>G	XP_005264316.1:p.Asp417Gly
XM_011532764.1:c.428A>G	XP_011531066.1:p.Asp143Gly
XM_011532765.1:c.428A>G	XP_011531067.1:p.Asp143Gly
XR_939677.1:n.1315A>G
XM_005264259.5:c.1250A>G	XP_005264316.1:p.Asp417Gly
XM_011532764.3:c.428A>G	XP_011531066.1:p.Asp143Gly
XM_011532765.3:c.428A>G	XP_011531067.1:p.Asp143Gly
XM_017003803.2:c.1079A>G	XP_016859292.1:p.Asp360Gly
XR_001738703.2:n.1315A>G
NM_000821.7:c.1250A>G MANE Select	NP_000812.2:p.Asp417Gly
NM_001142269.4:c.1079A>G	NP_001135741.1:p.Asp360Gly