Canonical Allele Identifier: CA427440129

Gene: GGCX

Linked Data

• MyVariant Identifiers: chr2:g.85779077C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85551954C>T , CM000664.2:g.85551954C>T	GRCh38
NC_000002.11:g.85779077C>T , CM000664.1:g.85779077C>T	GRCh37
NC_000002.10:g.85632588C>T	NCBI36
NG_011811.2:g.14581G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000473665.2:n.5945G>A
ENST00000482662.2:n.4352G>A
ENST00000685865.1:n.2304G>A
ENST00000687250.1:n.2004G>A
ENST00000687995.1:n.1819G>A
ENST00000688205.1:c.*1060G>A	ENSP00000509673.1:n.*1060G>A
ENST00000688788.1:n.1706G>A
ENST00000689276.1:c.1398G>A	ENSP00000510012.1:p.Val466=
ENST00000689576.1:c.*86G>A	ENSP00000508712.1:n.*86G>A
ENST00000690108.1:c.*1123G>A	ENSP00000510617.1:n.*1123G>A
ENST00000690468.1:c.*19G>A	ENSP00000509078.1:n.*19G>A
ENST00000690595.1:c.792G>A	ENSP00000508979.1:p.Val264=
ENST00000691348.1:c.*19G>A	ENSP00000509369.1:n.*19G>A
ENST00000691410.1:c.*1044G>A	ENSP00000508479.1:n.*1044G>A
ENST00000693287.1:c.783G>A	ENSP00000510264.1:p.Val261=
ENST00000693681.1:c.780G>A	ENSP00000510789.1:p.Val260=
ENST00000233838.9:c.1467G>A MANE Select	ENSP00000233838.3:p.Val489=
ENST00000233838.8:c.1467G>A	ENSP00000233838.3:p.Val489=
ENST00000430215.7:c.1296G>A	ENSP00000408045.3:p.Val432=
ENST00000465637.5:n.179-3950G>A
NM_000821.5:c.1467G>A	NP_000812.2:p.Val489=
NM_000821.6:c.1467G>A	NP_000812.2:p.Val489=
NM_001142269.2:c.1296G>A	NP_001135741.1:p.Val432=
NM_001142269.3:c.1296G>A	NP_001135741.1:p.Val432=
XM_005264259.3:c.1467G>A	XP_005264316.1:p.Val489=
XM_011532764.1:c.645G>A	XP_011531066.1:p.Val215=
XM_011532765.1:c.645G>A	XP_011531067.1:p.Val215=
XR_939677.1:n.1380G>A
XM_005264259.5:c.1467G>A	XP_005264316.1:p.Val489=
XM_011532764.3:c.645G>A	XP_011531066.1:p.Val215=
XM_011532765.3:c.645G>A	XP_011531067.1:p.Val215=
XM_017003803.2:c.1296G>A	XP_016859292.1:p.Val432=
XR_001738703.2:n.1380G>A
NM_000821.7:c.1467G>A MANE Select	NP_000812.2:p.Val489=
NM_001142269.4:c.1296G>A	NP_001135741.1:p.Val432=