Canonical Allele Identifier: CA347484766

Gene: GGCX

Linked Data

• MyVariant Identifiers: chr2:g.85778958A>T (hg19) ; chr2:g.85551835A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85551835A>T , CM000664.2:g.85551835A>T	GRCh38
NC_000002.11:g.85778958A>T , CM000664.1:g.85778958A>T	GRCh37
NC_000002.10:g.85632469A>T	NCBI36
NG_011811.2:g.14700T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000473665.2:n.6064T>A
ENST00000482662.2:n.4471T>A
ENST00000685865.1:n.2423T>A
ENST00000687250.1:n.2123T>A
ENST00000687995.1:n.1938T>A
ENST00000688205.1:c.*1179T>A	ENSP00000509673.1:n.*1179T>A
ENST00000688788.1:n.1825T>A
ENST00000689276.1:c.1517T>A	ENSP00000510012.1:p.Val506Glu
ENST00000689576.1:c.*205T>A	ENSP00000508712.1:n.*205T>A
ENST00000690108.1:c.*1242T>A	ENSP00000510617.1:n.*1242T>A
ENST00000690468.1:c.*138T>A	ENSP00000509078.1:n.*138T>A
ENST00000690595.1:c.911T>A	ENSP00000508979.1:p.Val304Glu
ENST00000691348.1:c.*138T>A	ENSP00000509369.1:n.*138T>A
ENST00000691410.1:c.*1163T>A	ENSP00000508479.1:n.*1163T>A
ENST00000693287.1:c.902T>A	ENSP00000510264.1:p.Val301Glu
ENST00000693681.1:c.899T>A	ENSP00000510789.1:p.Val300Glu
ENST00000233838.9:c.1586T>A MANE Select	ENSP00000233838.3:p.Val529Glu
ENST00000233838.8:c.1586T>A	ENSP00000233838.3:p.Val529Glu
ENST00000430215.7:c.1415T>A	ENSP00000408045.3:p.Val472Glu
ENST00000465637.5:n.179-3831T>A
NM_000821.5:c.1586T>A	NP_000812.2:p.Val529Glu
NM_000821.6:c.1586T>A	NP_000812.2:p.Val529Glu
NM_001142269.2:c.1415T>A	NP_001135741.1:p.Val472Glu
NM_001142269.3:c.1415T>A	NP_001135741.1:p.Val472Glu
XM_005264259.3:c.1586T>A	XP_005264316.1:p.Val529Glu
XM_011532764.1:c.764T>A	XP_011531066.1:p.Val255Glu
XM_011532765.1:c.764T>A	XP_011531067.1:p.Val255Glu
XR_939677.1:n.1499T>A
XM_005264259.5:c.1586T>A	XP_005264316.1:p.Val529Glu
XM_011532764.3:c.764T>A	XP_011531066.1:p.Val255Glu
XM_011532765.3:c.764T>A	XP_011531067.1:p.Val255Glu
XM_017003803.2:c.1415T>A	XP_016859292.1:p.Val472Glu
XR_001738703.2:n.1499T>A
NM_000821.7:c.1586T>A MANE Select	NP_000812.2:p.Val529Glu
NM_001142269.4:c.1415T>A	NP_001135741.1:p.Val472Glu