Canonical Allele Identifier: CA427440097

Gene: GGCX

Linked Data

• MyVariant Identifiers: chr2:g.85779032T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85551909T>C , CM000664.2:g.85551909T>C	GRCh38
NC_000002.11:g.85779032T>C , CM000664.1:g.85779032T>C	GRCh37
NC_000002.10:g.85632543T>C	NCBI36
NG_011811.2:g.14626A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000473665.2:n.5990A>G
ENST00000482662.2:n.4397A>G
ENST00000685865.1:n.2349A>G
ENST00000687250.1:n.2049A>G
ENST00000687995.1:n.1864A>G
ENST00000688205.1:c.*1105A>G	ENSP00000509673.1:n.*1105A>G
ENST00000688788.1:n.1751A>G
ENST00000689276.1:c.1443A>G	ENSP00000510012.1:p.Pro481=
ENST00000689576.1:c.*131A>G	ENSP00000508712.1:n.*131A>G
ENST00000690108.1:c.*1168A>G	ENSP00000510617.1:n.*1168A>G
ENST00000690468.1:c.*64A>G	ENSP00000509078.1:n.*64A>G
ENST00000690595.1:c.837A>G	ENSP00000508979.1:p.Pro279=
ENST00000691348.1:c.*64A>G	ENSP00000509369.1:n.*64A>G
ENST00000691410.1:c.*1089A>G	ENSP00000508479.1:n.*1089A>G
ENST00000693287.1:c.828A>G	ENSP00000510264.1:p.Pro276=
ENST00000693681.1:c.825A>G	ENSP00000510789.1:p.Pro275=
ENST00000233838.9:c.1512A>G MANE Select	ENSP00000233838.3:p.Pro504=
ENST00000233838.8:c.1512A>G	ENSP00000233838.3:p.Pro504=
ENST00000430215.7:c.1341A>G	ENSP00000408045.3:p.Pro447=
ENST00000465637.5:n.179-3905A>G
NM_000821.5:c.1512A>G	NP_000812.2:p.Pro504=
NM_000821.6:c.1512A>G	NP_000812.2:p.Pro504=
NM_001142269.2:c.1341A>G	NP_001135741.1:p.Pro447=
NM_001142269.3:c.1341A>G	NP_001135741.1:p.Pro447=
XM_005264259.3:c.1512A>G	XP_005264316.1:p.Pro504=
XM_011532764.1:c.690A>G	XP_011531066.1:p.Pro230=
XM_011532765.1:c.690A>G	XP_011531067.1:p.Pro230=
XR_939677.1:n.1425A>G
XM_005264259.5:c.1512A>G	XP_005264316.1:p.Pro504=
XM_011532764.3:c.690A>G	XP_011531066.1:p.Pro230=
XM_011532765.3:c.690A>G	XP_011531067.1:p.Pro230=
XM_017003803.2:c.1341A>G	XP_016859292.1:p.Pro447=
XR_001738703.2:n.1425A>G
NM_000821.7:c.1512A>G MANE Select	NP_000812.2:p.Pro504=
NM_001142269.4:c.1341A>G	NP_001135741.1:p.Pro447=