Canonical Allele Identifier: CA347487199

Gene: GGCX

Linked Data

• MyVariant Identifiers: chr2:g.85780186T>C (hg19) ; chr2:g.85553063T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85553063T>C , CM000664.2:g.85553063T>C	GRCh38
NC_000002.11:g.85780186T>C , CM000664.1:g.85780186T>C	GRCh37
NC_000002.10:g.85633697T>C	NCBI36
NG_011811.2:g.13472A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000473665.2:n.5207A>G
ENST00000482662.2:n.3614A>G
ENST00000685865.1:n.1566A>G
ENST00000687250.1:n.1266A>G
ENST00000687995.1:n.1515A>G
ENST00000688205.1:c.*756A>G	ENSP00000509673.1:n.*756A>G
ENST00000688788.1:n.1402A>G
ENST00000689276.1:c.1094A>G	ENSP00000510012.1:p.Asn365Ser
ENST00000689576.1:c.1163A>G	ENSP00000508712.1:p.Asn388Ser
ENST00000690108.1:c.*819A>G	ENSP00000510617.1:n.*819A>G
ENST00000690468.1:c.884A>G	ENSP00000509078.1:p.Asn295Ser
ENST00000690595.1:c.488A>G	ENSP00000508979.1:p.Asn163Ser
ENST00000691348.1:c.992A>G	ENSP00000509369.1:p.Asn331Ser
ENST00000691410.1:c.*740A>G	ENSP00000508479.1:n.*740A>G
ENST00000693287.1:c.479A>G	ENSP00000510264.1:p.Asn160Ser
ENST00000693681.1:c.476A>G	ENSP00000510789.1:p.Asn159Ser
ENST00000233838.9:c.1163A>G MANE Select	ENSP00000233838.3:p.Asn388Ser
ENST00000233838.8:c.1163A>G	ENSP00000233838.3:p.Asn388Ser
ENST00000430215.7:c.992A>G	ENSP00000408045.3:p.Asn331Ser
ENST00000465637.5:n.179-5059A>G
ENST00000473665.1:n.656A>G
ENST00000482662.1:n.580A>G
NM_000821.5:c.1163A>G	NP_000812.2:p.Asn388Ser
NM_000821.6:c.1163A>G	NP_000812.2:p.Asn388Ser
NM_001142269.2:c.992A>G	NP_001135741.1:p.Asn331Ser
NM_001142269.3:c.992A>G	NP_001135741.1:p.Asn331Ser
XM_005264259.3:c.1163A>G	XP_005264316.1:p.Asn388Ser
XM_011532764.1:c.341A>G	XP_011531066.1:p.Asn114Ser
XM_011532765.1:c.341A>G	XP_011531067.1:p.Asn114Ser
XR_939677.1:n.1228A>G
XM_005264259.5:c.1163A>G	XP_005264316.1:p.Asn388Ser
XM_011532764.3:c.341A>G	XP_011531066.1:p.Asn114Ser
XM_011532765.3:c.341A>G	XP_011531067.1:p.Asn114Ser
XM_017003803.2:c.992A>G	XP_016859292.1:p.Asn331Ser
XR_001738703.2:n.1228A>G
NM_000821.7:c.1163A>G MANE Select	NP_000812.2:p.Asn388Ser
NM_001142269.4:c.992A>G	NP_001135741.1:p.Asn331Ser