Canonical Allele Identifier: CA347484840

Gene: GGCX

Linked Data

• MyVariant Identifiers: chr2:g.85778989T>G (hg19) ; chr2:g.85551866T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85551866T>G , CM000664.2:g.85551866T>G	GRCh38
NC_000002.11:g.85778989T>G , CM000664.1:g.85778989T>G	GRCh37
NC_000002.10:g.85632500T>G	NCBI36
NG_011811.2:g.14669A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000473665.2:n.6033A>C
ENST00000482662.2:n.4440A>C
ENST00000685865.1:n.2392A>C
ENST00000687250.1:n.2092A>C
ENST00000687995.1:n.1907A>C
ENST00000688205.1:c.*1148A>C	ENSP00000509673.1:n.*1148A>C
ENST00000688788.1:n.1794A>C
ENST00000689276.1:c.1486A>C	ENSP00000510012.1:p.Ile496Leu
ENST00000689576.1:c.*174A>C	ENSP00000508712.1:n.*174A>C
ENST00000690108.1:c.*1211A>C	ENSP00000510617.1:n.*1211A>C
ENST00000690468.1:c.*107A>C	ENSP00000509078.1:n.*107A>C
ENST00000690595.1:c.880A>C	ENSP00000508979.1:p.Ile294Leu
ENST00000691348.1:c.*107A>C	ENSP00000509369.1:n.*107A>C
ENST00000691410.1:c.*1132A>C	ENSP00000508479.1:n.*1132A>C
ENST00000693287.1:c.871A>C	ENSP00000510264.1:p.Ile291Leu
ENST00000693681.1:c.868A>C	ENSP00000510789.1:p.Ile290Leu
ENST00000233838.9:c.1555A>C MANE Select	ENSP00000233838.3:p.Ile519Leu
ENST00000233838.8:c.1555A>C	ENSP00000233838.3:p.Ile519Leu
ENST00000430215.7:c.1384A>C	ENSP00000408045.3:p.Ile462Leu
ENST00000465637.5:n.179-3862A>C
NM_000821.5:c.1555A>C	NP_000812.2:p.Ile519Leu
NM_000821.6:c.1555A>C	NP_000812.2:p.Ile519Leu
NM_001142269.2:c.1384A>C	NP_001135741.1:p.Ile462Leu
NM_001142269.3:c.1384A>C	NP_001135741.1:p.Ile462Leu
XM_005264259.3:c.1555A>C	XP_005264316.1:p.Ile519Leu
XM_011532764.1:c.733A>C	XP_011531066.1:p.Ile245Leu
XM_011532765.1:c.733A>C	XP_011531067.1:p.Ile245Leu
XR_939677.1:n.1468A>C
XM_005264259.5:c.1555A>C	XP_005264316.1:p.Ile519Leu
XM_011532764.3:c.733A>C	XP_011531066.1:p.Ile245Leu
XM_011532765.3:c.733A>C	XP_011531067.1:p.Ile245Leu
XM_017003803.2:c.1384A>C	XP_016859292.1:p.Ile462Leu
XR_001738703.2:n.1468A>C
NM_000821.7:c.1555A>C MANE Select	NP_000812.2:p.Ile519Leu
NM_001142269.4:c.1384A>C	NP_001135741.1:p.Ile462Leu