Canonical Allele Identifier: CA427440105

Gene: GGCX

Linked Data

• MyVariant Identifiers: chr2:g.85779044G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85551921G>T , CM000664.2:g.85551921G>T	GRCh38
NC_000002.11:g.85779044G>T , CM000664.1:g.85779044G>T	GRCh37
NC_000002.10:g.85632555G>T	NCBI36
NG_011811.2:g.14614C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000473665.2:n.5978C>A
ENST00000482662.2:n.4385C>A
ENST00000685865.1:n.2337C>A
ENST00000687250.1:n.2037C>A
ENST00000687995.1:n.1852C>A
ENST00000688205.1:c.*1093C>A	ENSP00000509673.1:n.*1093C>A
ENST00000688788.1:n.1739C>A
ENST00000689276.1:c.1431C>A	ENSP00000510012.1:p.Ser477=
ENST00000689576.1:c.*119C>A	ENSP00000508712.1:n.*119C>A
ENST00000690108.1:c.*1156C>A	ENSP00000510617.1:n.*1156C>A
ENST00000690468.1:c.*52C>A	ENSP00000509078.1:n.*52C>A
ENST00000690595.1:c.825C>A	ENSP00000508979.1:p.Ser275=
ENST00000691348.1:c.*52C>A	ENSP00000509369.1:n.*52C>A
ENST00000691410.1:c.*1077C>A	ENSP00000508479.1:n.*1077C>A
ENST00000693287.1:c.816C>A	ENSP00000510264.1:p.Ser272=
ENST00000693681.1:c.813C>A	ENSP00000510789.1:p.Ser271=
ENST00000233838.9:c.1500C>A MANE Select	ENSP00000233838.3:p.Ser500=
ENST00000233838.8:c.1500C>A	ENSP00000233838.3:p.Ser500=
ENST00000430215.7:c.1329C>A	ENSP00000408045.3:p.Ser443=
ENST00000465637.5:n.179-3917C>A
NM_000821.5:c.1500C>A	NP_000812.2:p.Ser500=
NM_000821.6:c.1500C>A	NP_000812.2:p.Ser500=
NM_001142269.2:c.1329C>A	NP_001135741.1:p.Ser443=
NM_001142269.3:c.1329C>A	NP_001135741.1:p.Ser443=
XM_005264259.3:c.1500C>A	XP_005264316.1:p.Ser500=
XM_011532764.1:c.678C>A	XP_011531066.1:p.Ser226=
XM_011532765.1:c.678C>A	XP_011531067.1:p.Ser226=
XR_939677.1:n.1413C>A
XM_005264259.5:c.1500C>A	XP_005264316.1:p.Ser500=
XM_011532764.3:c.678C>A	XP_011531066.1:p.Ser226=
XM_011532765.3:c.678C>A	XP_011531067.1:p.Ser226=
XM_017003803.2:c.1329C>A	XP_016859292.1:p.Ser443=
XR_001738703.2:n.1413C>A
NM_000821.7:c.1500C>A MANE Select	NP_000812.2:p.Ser500=
NM_001142269.4:c.1329C>A	NP_001135741.1:p.Ser443=