Canonical Allele Identifier: CA427440107

Gene: GGCX

Linked Data

• MyVariant Identifiers: chr2:g.85779047T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85551924T>C , CM000664.2:g.85551924T>C	GRCh38
NC_000002.11:g.85779047T>C , CM000664.1:g.85779047T>C	GRCh37
NC_000002.10:g.85632558T>C	NCBI36
NG_011811.2:g.14611A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000473665.2:n.5975A>G
ENST00000482662.2:n.4382A>G
ENST00000685865.1:n.2334A>G
ENST00000687250.1:n.2034A>G
ENST00000687995.1:n.1849A>G
ENST00000688205.1:c.*1090A>G	ENSP00000509673.1:n.*1090A>G
ENST00000688788.1:n.1736A>G
ENST00000689276.1:c.1428A>G	ENSP00000510012.1:p.Thr476=
ENST00000689576.1:c.*116A>G	ENSP00000508712.1:n.*116A>G
ENST00000690108.1:c.*1153A>G	ENSP00000510617.1:n.*1153A>G
ENST00000690468.1:c.*49A>G	ENSP00000509078.1:n.*49A>G
ENST00000690595.1:c.822A>G	ENSP00000508979.1:p.Thr274=
ENST00000691348.1:c.*49A>G	ENSP00000509369.1:n.*49A>G
ENST00000691410.1:c.*1074A>G	ENSP00000508479.1:n.*1074A>G
ENST00000693287.1:c.813A>G	ENSP00000510264.1:p.Thr271=
ENST00000693681.1:c.810A>G	ENSP00000510789.1:p.Thr270=
ENST00000233838.9:c.1497A>G MANE Select	ENSP00000233838.3:p.Thr499=
ENST00000233838.8:c.1497A>G	ENSP00000233838.3:p.Thr499=
ENST00000430215.7:c.1326A>G	ENSP00000408045.3:p.Thr442=
ENST00000465637.5:n.179-3920A>G
NM_000821.5:c.1497A>G	NP_000812.2:p.Thr499=
NM_000821.6:c.1497A>G	NP_000812.2:p.Thr499=
NM_001142269.2:c.1326A>G	NP_001135741.1:p.Thr442=
NM_001142269.3:c.1326A>G	NP_001135741.1:p.Thr442=
XM_005264259.3:c.1497A>G	XP_005264316.1:p.Thr499=
XM_011532764.1:c.675A>G	XP_011531066.1:p.Thr225=
XM_011532765.1:c.675A>G	XP_011531067.1:p.Thr225=
XR_939677.1:n.1410A>G
XM_005264259.5:c.1497A>G	XP_005264316.1:p.Thr499=
XM_011532764.3:c.675A>G	XP_011531066.1:p.Thr225=
XM_011532765.3:c.675A>G	XP_011531067.1:p.Thr225=
XM_017003803.2:c.1326A>G	XP_016859292.1:p.Thr442=
XR_001738703.2:n.1410A>G
NM_000821.7:c.1497A>G MANE Select	NP_000812.2:p.Thr499=
NM_001142269.4:c.1326A>G	NP_001135741.1:p.Thr442=