Canonical Allele Identifier: CA347489260

Gene: GGCX

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85554259C>T , CM000664.2:g.85554259C>T	GRCh38
NC_000002.11:g.85781382C>T , CM000664.1:g.85781382C>T	GRCh37
NC_000002.10:g.85634893C>T	NCBI36
NG_011811.2:g.12276G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000821.7:c.773G>A MANE Select	NP_000812.2:p.Gly258Asp
ENST00000233838.9:c.773G>A MANE Select	ENSP00000233838.3:p.Gly258Asp
NM_000821.5:c.773G>A	NP_000812.2:p.Gly258Asp
NM_000821.6:c.773G>A	NP_000812.2:p.Gly258Asp
NM_001142269.2:c.602G>A	NP_001135741.1:p.Gly201Asp
NM_001142269.3:c.602G>A	NP_001135741.1:p.Gly201Asp
NM_001142269.4:c.602G>A	NP_001135741.1:p.Gly201Asp
ENST00000233838.8:c.773G>A	ENSP00000233838.3:p.Gly258Asp
ENST00000430215.7:c.602G>A	ENSP00000408045.3:p.Gly201Asp
ENST00000465637.5:n.178+4747G>A
ENST00000473665.1:n.266G>A
ENST00000473665.2:n.4817G>A
ENST00000482662.2:n.2579G>A
ENST00000685865.1:n.1176G>A
ENST00000687250.1:n.876G>A
ENST00000687995.1:n.1125G>A
ENST00000688205.1:c.*366G>A	ENSP00000509673.1:n.*366G>A
ENST00000688788.1:n.1129-762G>A
ENST00000689276.1:c.704G>A	ENSP00000510012.1:p.Gly235Asp
ENST00000689576.1:c.773G>A	ENSP00000508712.1:p.Gly258Asp
ENST00000690108.1:c.*429G>A	ENSP00000510617.1:n.*429G>A
ENST00000690468.1:c.494G>A	ENSP00000509078.1:p.Gly165Asp
ENST00000690595.1:c.215-762G>A	ENSP00000508979.1:n.215-762G>A
ENST00000691348.1:c.602G>A	ENSP00000509369.1:p.Gly201Asp
ENST00000691410.1:c.*350G>A	ENSP00000508479.1:n.*350G>A
ENST00000693287.1:c.89G>A	ENSP00000510264.1:p.Gly30Asp
ENST00000693681.1:c.203-762G>A	ENSP00000510789.1:n.203-762G>A
XM_005264259.3:c.773G>A	XP_005264316.1:p.Gly258Asp
XM_005264259.5:c.773G>A	XP_005264316.1:p.Gly258Asp
XM_011532764.1:c.68-762G>A	XP_011531066.1:n.68-762G>A
XM_011532764.3:c.68-762G>A	XP_011531066.1:n.68-762G>A
XM_011532765.1:c.68-762G>A	XP_011531067.1:n.68-762G>A
XM_011532765.3:c.68-762G>A	XP_011531067.1:n.68-762G>A
XM_017003803.2:c.602G>A	XP_016859292.1:p.Gly201Asp
XR_001738703.2:n.838G>A
XR_939677.1:n.838G>A