Canonical Allele Identifier: CA347484940

Gene: GGCX

Linked Data

• MyVariant Identifiers: chr2:g.85779034G>T (hg19) ; chr2:g.85551911G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85551911G>T , CM000664.2:g.85551911G>T	GRCh38
NC_000002.11:g.85779034G>T , CM000664.1:g.85779034G>T	GRCh37
NC_000002.10:g.85632545G>T	NCBI36
NG_011811.2:g.14624C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000473665.2:n.5988C>A
ENST00000482662.2:n.4395C>A
ENST00000685865.1:n.2347C>A
ENST00000687250.1:n.2047C>A
ENST00000687995.1:n.1862C>A
ENST00000688205.1:c.*1103C>A	ENSP00000509673.1:n.*1103C>A
ENST00000688788.1:n.1749C>A
ENST00000689276.1:c.1441C>A	ENSP00000510012.1:p.Pro481Thr
ENST00000689576.1:c.*129C>A	ENSP00000508712.1:n.*129C>A
ENST00000690108.1:c.*1166C>A	ENSP00000510617.1:n.*1166C>A
ENST00000690468.1:c.*62C>A	ENSP00000509078.1:n.*62C>A
ENST00000690595.1:c.835C>A	ENSP00000508979.1:p.Pro279Thr
ENST00000691348.1:c.*62C>A	ENSP00000509369.1:n.*62C>A
ENST00000691410.1:c.*1087C>A	ENSP00000508479.1:n.*1087C>A
ENST00000693287.1:c.826C>A	ENSP00000510264.1:p.Pro276Thr
ENST00000693681.1:c.823C>A	ENSP00000510789.1:p.Pro275Thr
ENST00000233838.9:c.1510C>A MANE Select	ENSP00000233838.3:p.Pro504Thr
ENST00000233838.8:c.1510C>A	ENSP00000233838.3:p.Pro504Thr
ENST00000430215.7:c.1339C>A	ENSP00000408045.3:p.Pro447Thr
ENST00000465637.5:n.179-3907C>A
NM_000821.5:c.1510C>A	NP_000812.2:p.Pro504Thr
NM_000821.6:c.1510C>A	NP_000812.2:p.Pro504Thr
NM_001142269.2:c.1339C>A	NP_001135741.1:p.Pro447Thr
NM_001142269.3:c.1339C>A	NP_001135741.1:p.Pro447Thr
XM_005264259.3:c.1510C>A	XP_005264316.1:p.Pro504Thr
XM_011532764.1:c.688C>A	XP_011531066.1:p.Pro230Thr
XM_011532765.1:c.688C>A	XP_011531067.1:p.Pro230Thr
XR_939677.1:n.1423C>A
XM_005264259.5:c.1510C>A	XP_005264316.1:p.Pro504Thr
XM_011532764.3:c.688C>A	XP_011531066.1:p.Pro230Thr
XM_011532765.3:c.688C>A	XP_011531067.1:p.Pro230Thr
XM_017003803.2:c.1339C>A	XP_016859292.1:p.Pro447Thr
XR_001738703.2:n.1423C>A
NM_000821.7:c.1510C>A MANE Select	NP_000812.2:p.Pro504Thr
NM_001142269.4:c.1339C>A	NP_001135741.1:p.Pro447Thr