Canonical Allele Identifier: CA427440152

Gene: GGCX

Linked Data

• COSMIC: COSM1023364
• MyVariant Identifiers: chr2:g.85779092A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85551969A>G , CM000664.2:g.85551969A>G	GRCh38
NC_000002.11:g.85779092A>G , CM000664.1:g.85779092A>G	GRCh37
NC_000002.10:g.85632603A>G	NCBI36
NG_011811.2:g.14566T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000473665.2:n.5930T>C
ENST00000482662.2:n.4337T>C
ENST00000685865.1:n.2289T>C
ENST00000687250.1:n.1989T>C
ENST00000687995.1:n.1804T>C
ENST00000688205.1:c.*1045T>C	ENSP00000509673.1:n.*1045T>C
ENST00000688788.1:n.1691T>C
ENST00000689276.1:c.1383T>C	ENSP00000510012.1:p.Pro461=
ENST00000689576.1:c.*71T>C	ENSP00000508712.1:n.*71T>C
ENST00000690108.1:c.*1108T>C	ENSP00000510617.1:n.*1108T>C
ENST00000690468.1:c.*4T>C	ENSP00000509078.1:n.*4T>C
ENST00000690595.1:c.777T>C	ENSP00000508979.1:p.Pro259=
ENST00000691348.1:c.*4T>C	ENSP00000509369.1:n.*4T>C
ENST00000691410.1:c.*1029T>C	ENSP00000508479.1:n.*1029T>C
ENST00000693287.1:c.768T>C	ENSP00000510264.1:p.Pro256=
ENST00000693681.1:c.765T>C	ENSP00000510789.1:p.Pro255=
ENST00000233838.9:c.1452T>C MANE Select	ENSP00000233838.3:p.Pro484=
ENST00000233838.8:c.1452T>C	ENSP00000233838.3:p.Pro484=
ENST00000430215.7:c.1281T>C	ENSP00000408045.3:p.Pro427=
ENST00000465637.5:n.179-3965T>C
NM_000821.5:c.1452T>C	NP_000812.2:p.Pro484=
NM_000821.6:c.1452T>C	NP_000812.2:p.Pro484=
NM_001142269.2:c.1281T>C	NP_001135741.1:p.Pro427=
NM_001142269.3:c.1281T>C	NP_001135741.1:p.Pro427=
XM_005264259.3:c.1452T>C	XP_005264316.1:p.Pro484=
XM_011532764.1:c.630T>C	XP_011531066.1:p.Pro210=
XM_011532765.1:c.630T>C	XP_011531067.1:p.Pro210=
XR_939677.1:n.1365T>C
XM_005264259.5:c.1452T>C	XP_005264316.1:p.Pro484=
XM_011532764.3:c.630T>C	XP_011531066.1:p.Pro210=
XM_011532765.3:c.630T>C	XP_011531067.1:p.Pro210=
XM_017003803.2:c.1281T>C	XP_016859292.1:p.Pro427=
XR_001738703.2:n.1365T>C
NM_000821.7:c.1452T>C MANE Select	NP_000812.2:p.Pro484=
NM_001142269.4:c.1281T>C	NP_001135741.1:p.Pro427=