Canonical Allele Identifier: CA427085186

Gene: GGCX

Linked Data

• MyVariant Identifiers: chr2:g.85780110G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85552987G>T , CM000664.2:g.85552987G>T	GRCh38
NC_000002.11:g.85780110G>T , CM000664.1:g.85780110G>T	GRCh37
NC_000002.10:g.85633621G>T	NCBI36
NG_011811.2:g.13548C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000473665.2:n.5283C>A
ENST00000482662.2:n.3690C>A
ENST00000685865.1:n.1642C>A
ENST00000687250.1:n.1342C>A
ENST00000687995.1:n.1591C>A
ENST00000688205.1:c.*832C>A	ENSP00000509673.1:n.*832C>A
ENST00000688788.1:n.1478C>A
ENST00000689276.1:c.1170C>A	ENSP00000510012.1:p.Ile390=
ENST00000689576.1:c.1239C>A	ENSP00000508712.1:p.Ile413=
ENST00000690108.1:c.*895C>A	ENSP00000510617.1:n.*895C>A
ENST00000690468.1:c.960C>A	ENSP00000509078.1:p.Ile320=
ENST00000690595.1:c.564C>A	ENSP00000508979.1:p.Ile188=
ENST00000691348.1:c.1068C>A	ENSP00000509369.1:p.Ile356=
ENST00000691410.1:c.*816C>A	ENSP00000508479.1:n.*816C>A
ENST00000693287.1:c.555C>A	ENSP00000510264.1:p.Ile185=
ENST00000693681.1:c.552C>A	ENSP00000510789.1:p.Ile184=
ENST00000233838.9:c.1239C>A MANE Select	ENSP00000233838.3:p.Ile413=
ENST00000233838.8:c.1239C>A	ENSP00000233838.3:p.Ile413=
ENST00000430215.7:c.1068C>A	ENSP00000408045.3:p.Ile356=
ENST00000465637.5:n.179-4983C>A
ENST00000473665.1:n.732C>A
ENST00000482662.1:n.656C>A
NM_000821.5:c.1239C>A	NP_000812.2:p.Ile413=
NM_000821.6:c.1239C>A	NP_000812.2:p.Ile413=
NM_001142269.2:c.1068C>A	NP_001135741.1:p.Ile356=
NM_001142269.3:c.1068C>A	NP_001135741.1:p.Ile356=
XM_005264259.3:c.1239C>A	XP_005264316.1:p.Ile413=
XM_011532764.1:c.417C>A	XP_011531066.1:p.Ile139=
XM_011532765.1:c.417C>A	XP_011531067.1:p.Ile139=
XR_939677.1:n.1304C>A
XM_005264259.5:c.1239C>A	XP_005264316.1:p.Ile413=
XM_011532764.3:c.417C>A	XP_011531066.1:p.Ile139=
XM_011532765.3:c.417C>A	XP_011531067.1:p.Ile139=
XM_017003803.2:c.1068C>A	XP_016859292.1:p.Ile356=
XR_001738703.2:n.1304C>A
NM_000821.7:c.1239C>A MANE Select	NP_000812.2:p.Ile413=
NM_001142269.4:c.1068C>A	NP_001135741.1:p.Ile356=