Canonical Allele Identifier: CA427440122

Gene: GGCX

Linked Data

• MyVariant Identifiers: chr2:g.85779071G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85551948G>T , CM000664.2:g.85551948G>T	GRCh38
NC_000002.11:g.85779071G>T , CM000664.1:g.85779071G>T	GRCh37
NC_000002.10:g.85632582G>T	NCBI36
NG_011811.2:g.14587C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000473665.2:n.5951C>A
ENST00000482662.2:n.4358C>A
ENST00000685865.1:n.2310C>A
ENST00000687250.1:n.2010C>A
ENST00000687995.1:n.1825C>A
ENST00000688205.1:c.*1066C>A	ENSP00000509673.1:n.*1066C>A
ENST00000688788.1:n.1712C>A
ENST00000689276.1:c.1404C>A	ENSP00000510012.1:p.Ala468=
ENST00000689576.1:c.*92C>A	ENSP00000508712.1:n.*92C>A
ENST00000690108.1:c.*1129C>A	ENSP00000510617.1:n.*1129C>A
ENST00000690468.1:c.*25C>A	ENSP00000509078.1:n.*25C>A
ENST00000690595.1:c.798C>A	ENSP00000508979.1:p.Ala266=
ENST00000691348.1:c.*25C>A	ENSP00000509369.1:n.*25C>A
ENST00000691410.1:c.*1050C>A	ENSP00000508479.1:n.*1050C>A
ENST00000693287.1:c.789C>A	ENSP00000510264.1:p.Ala263=
ENST00000693681.1:c.786C>A	ENSP00000510789.1:p.Ala262=
ENST00000233838.9:c.1473C>A MANE Select	ENSP00000233838.3:p.Ala491=
ENST00000233838.8:c.1473C>A	ENSP00000233838.3:p.Ala491=
ENST00000430215.7:c.1302C>A	ENSP00000408045.3:p.Ala434=
ENST00000465637.5:n.179-3944C>A
NM_000821.5:c.1473C>A	NP_000812.2:p.Ala491=
NM_000821.6:c.1473C>A	NP_000812.2:p.Ala491=
NM_001142269.2:c.1302C>A	NP_001135741.1:p.Ala434=
NM_001142269.3:c.1302C>A	NP_001135741.1:p.Ala434=
XM_005264259.3:c.1473C>A	XP_005264316.1:p.Ala491=
XM_011532764.1:c.651C>A	XP_011531066.1:p.Ala217=
XM_011532765.1:c.651C>A	XP_011531067.1:p.Ala217=
XR_939677.1:n.1386C>A
XM_005264259.5:c.1473C>A	XP_005264316.1:p.Ala491=
XM_011532764.3:c.651C>A	XP_011531066.1:p.Ala217=
XM_011532765.3:c.651C>A	XP_011531067.1:p.Ala217=
XM_017003803.2:c.1302C>A	XP_016859292.1:p.Ala434=
XR_001738703.2:n.1386C>A
NM_000821.7:c.1473C>A MANE Select	NP_000812.2:p.Ala491=
NM_001142269.4:c.1302C>A	NP_001135741.1:p.Ala434=