Canonical Allele Identifier: CA427440084

Gene: GGCX

Linked Data

• MyVariant Identifiers: chr2:g.85779014A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85551891A>G , CM000664.2:g.85551891A>G	GRCh38
NC_000002.11:g.85779014A>G , CM000664.1:g.85779014A>G	GRCh37
NC_000002.10:g.85632525A>G	NCBI36
NG_011811.2:g.14644T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000473665.2:n.6008T>C
ENST00000482662.2:n.4415T>C
ENST00000685865.1:n.2367T>C
ENST00000687250.1:n.2067T>C
ENST00000687995.1:n.1882T>C
ENST00000688205.1:c.*1123T>C	ENSP00000509673.1:n.*1123T>C
ENST00000688788.1:n.1769T>C
ENST00000689276.1:c.1461T>C	ENSP00000510012.1:p.Ser487=
ENST00000689576.1:c.*149T>C	ENSP00000508712.1:n.*149T>C
ENST00000690108.1:c.*1186T>C	ENSP00000510617.1:n.*1186T>C
ENST00000690468.1:c.*82T>C	ENSP00000509078.1:n.*82T>C
ENST00000690595.1:c.855T>C	ENSP00000508979.1:p.Ser285=
ENST00000691348.1:c.*82T>C	ENSP00000509369.1:n.*82T>C
ENST00000691410.1:c.*1107T>C	ENSP00000508479.1:n.*1107T>C
ENST00000693287.1:c.846T>C	ENSP00000510264.1:p.Ser282=
ENST00000693681.1:c.843T>C	ENSP00000510789.1:p.Ser281=
ENST00000233838.9:c.1530T>C MANE Select	ENSP00000233838.3:p.Ser510=
ENST00000233838.8:c.1530T>C	ENSP00000233838.3:p.Ser510=
ENST00000430215.7:c.1359T>C	ENSP00000408045.3:p.Ser453=
ENST00000465637.5:n.179-3887T>C
NM_000821.5:c.1530T>C	NP_000812.2:p.Ser510=
NM_000821.6:c.1530T>C	NP_000812.2:p.Ser510=
NM_001142269.2:c.1359T>C	NP_001135741.1:p.Ser453=
NM_001142269.3:c.1359T>C	NP_001135741.1:p.Ser453=
XM_005264259.3:c.1530T>C	XP_005264316.1:p.Ser510=
XM_011532764.1:c.708T>C	XP_011531066.1:p.Ser236=
XM_011532765.1:c.708T>C	XP_011531067.1:p.Ser236=
XR_939677.1:n.1443T>C
XM_005264259.5:c.1530T>C	XP_005264316.1:p.Ser510=
XM_011532764.3:c.708T>C	XP_011531066.1:p.Ser236=
XM_011532765.3:c.708T>C	XP_011531067.1:p.Ser236=
XM_017003803.2:c.1359T>C	XP_016859292.1:p.Ser453=
XR_001738703.2:n.1443T>C
NM_000821.7:c.1530T>C MANE Select	NP_000812.2:p.Ser510=
NM_001142269.4:c.1359T>C	NP_001135741.1:p.Ser453=