Canonical Allele Identifier: CA427440100

Gene: GGCX

Linked Data

• MyVariant Identifiers: chr2:g.85779038C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85551915C>A , CM000664.2:g.85551915C>A	GRCh38
NC_000002.11:g.85779038C>A , CM000664.1:g.85779038C>A	GRCh37
NC_000002.10:g.85632549C>A	NCBI36
NG_011811.2:g.14620G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000473665.2:n.5984G>T
ENST00000482662.2:n.4391G>T
ENST00000685865.1:n.2343G>T
ENST00000687250.1:n.2043G>T
ENST00000687995.1:n.1858G>T
ENST00000688205.1:c.*1099G>T	ENSP00000509673.1:n.*1099G>T
ENST00000688788.1:n.1745G>T
ENST00000689276.1:c.1437G>T	ENSP00000510012.1:p.Val479=
ENST00000689576.1:c.*125G>T	ENSP00000508712.1:n.*125G>T
ENST00000690108.1:c.*1162G>T	ENSP00000510617.1:n.*1162G>T
ENST00000690468.1:c.*58G>T	ENSP00000509078.1:n.*58G>T
ENST00000690595.1:c.831G>T	ENSP00000508979.1:p.Val277=
ENST00000691348.1:c.*58G>T	ENSP00000509369.1:n.*58G>T
ENST00000691410.1:c.*1083G>T	ENSP00000508479.1:n.*1083G>T
ENST00000693287.1:c.822G>T	ENSP00000510264.1:p.Val274=
ENST00000693681.1:c.819G>T	ENSP00000510789.1:p.Val273=
ENST00000233838.9:c.1506G>T MANE Select	ENSP00000233838.3:p.Val502=
ENST00000233838.8:c.1506G>T	ENSP00000233838.3:p.Val502=
ENST00000430215.7:c.1335G>T	ENSP00000408045.3:p.Val445=
ENST00000465637.5:n.179-3911G>T
NM_000821.5:c.1506G>T	NP_000812.2:p.Val502=
NM_000821.6:c.1506G>T	NP_000812.2:p.Val502=
NM_001142269.2:c.1335G>T	NP_001135741.1:p.Val445=
NM_001142269.3:c.1335G>T	NP_001135741.1:p.Val445=
XM_005264259.3:c.1506G>T	XP_005264316.1:p.Val502=
XM_011532764.1:c.684G>T	XP_011531066.1:p.Val228=
XM_011532765.1:c.684G>T	XP_011531067.1:p.Val228=
XR_939677.1:n.1419G>T
XM_005264259.5:c.1506G>T	XP_005264316.1:p.Val502=
XM_011532764.3:c.684G>T	XP_011531066.1:p.Val228=
XM_011532765.3:c.684G>T	XP_011531067.1:p.Val228=
XM_017003803.2:c.1335G>T	XP_016859292.1:p.Val445=
XR_001738703.2:n.1419G>T
NM_000821.7:c.1506G>T MANE Select	NP_000812.2:p.Val502=
NM_001142269.4:c.1335G>T	NP_001135741.1:p.Val445=