Canonical Allele Identifier: CA427440118

Gene: GGCX

Linked Data

• MyVariant Identifiers: chr2:g.85779062T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85551939T>G , CM000664.2:g.85551939T>G	GRCh38
NC_000002.11:g.85779062T>G , CM000664.1:g.85779062T>G	GRCh37
NC_000002.10:g.85632573T>G	NCBI36
NG_011811.2:g.14596A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000473665.2:n.5960A>C
ENST00000482662.2:n.4367A>C
ENST00000685865.1:n.2319A>C
ENST00000687250.1:n.2019A>C
ENST00000687995.1:n.1834A>C
ENST00000688205.1:c.*1075A>C	ENSP00000509673.1:n.*1075A>C
ENST00000688788.1:n.1721A>C
ENST00000689276.1:c.1413A>C	ENSP00000510012.1:p.Ser471=
ENST00000689576.1:c.*101A>C	ENSP00000508712.1:n.*101A>C
ENST00000690108.1:c.*1138A>C	ENSP00000510617.1:n.*1138A>C
ENST00000690468.1:c.*34A>C	ENSP00000509078.1:n.*34A>C
ENST00000690595.1:c.807A>C	ENSP00000508979.1:p.Ser269=
ENST00000691348.1:c.*34A>C	ENSP00000509369.1:n.*34A>C
ENST00000691410.1:c.*1059A>C	ENSP00000508479.1:n.*1059A>C
ENST00000693287.1:c.798A>C	ENSP00000510264.1:p.Ser266=
ENST00000693681.1:c.795A>C	ENSP00000510789.1:p.Ser265=
ENST00000233838.9:c.1482A>C MANE Select	ENSP00000233838.3:p.Ser494=
ENST00000233838.8:c.1482A>C	ENSP00000233838.3:p.Ser494=
ENST00000430215.7:c.1311A>C	ENSP00000408045.3:p.Ser437=
ENST00000465637.5:n.179-3935A>C
NM_000821.5:c.1482A>C	NP_000812.2:p.Ser494=
NM_000821.6:c.1482A>C	NP_000812.2:p.Ser494=
NM_001142269.2:c.1311A>C	NP_001135741.1:p.Ser437=
NM_001142269.3:c.1311A>C	NP_001135741.1:p.Ser437=
XM_005264259.3:c.1482A>C	XP_005264316.1:p.Ser494=
XM_011532764.1:c.660A>C	XP_011531066.1:p.Ser220=
XM_011532765.1:c.660A>C	XP_011531067.1:p.Ser220=
XR_939677.1:n.1395A>C
XM_005264259.5:c.1482A>C	XP_005264316.1:p.Ser494=
XM_011532764.3:c.660A>C	XP_011531066.1:p.Ser220=
XM_011532765.3:c.660A>C	XP_011531067.1:p.Ser220=
XM_017003803.2:c.1311A>C	XP_016859292.1:p.Ser437=
XR_001738703.2:n.1395A>C
NM_000821.7:c.1482A>C MANE Select	NP_000812.2:p.Ser494=
NM_001142269.4:c.1311A>C	NP_001135741.1:p.Ser437=