Canonical Allele Identifier: CA427085307

Gene: GGCX

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85553008G>C , CM000664.2:g.85553008G>C	GRCh38
NC_000002.11:g.85780131G>C , CM000664.1:g.85780131G>C	GRCh37
NC_000002.10:g.85633642G>C	NCBI36
NG_011811.2:g.13527C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000473665.2:n.5262C>G
ENST00000482662.2:n.3669C>G
ENST00000685865.1:n.1621C>G
ENST00000687250.1:n.1321C>G
ENST00000687995.1:n.1570C>G
ENST00000688205.1:c.*811C>G	ENSP00000509673.1:n.*811C>G
ENST00000688788.1:n.1457C>G
ENST00000689276.1:c.1149C>G	ENSP00000510012.1:p.Arg383=
ENST00000689576.1:c.1218C>G	ENSP00000508712.1:p.Arg406=
ENST00000690108.1:c.*874C>G	ENSP00000510617.1:n.*874C>G
ENST00000690468.1:c.939C>G	ENSP00000509078.1:p.Arg313=
ENST00000690595.1:c.543C>G	ENSP00000508979.1:p.Arg181=
ENST00000691348.1:c.1047C>G	ENSP00000509369.1:p.Arg349=
ENST00000691410.1:c.*795C>G	ENSP00000508479.1:n.*795C>G
ENST00000693287.1:c.534C>G	ENSP00000510264.1:p.Arg178=
ENST00000693681.1:c.531C>G	ENSP00000510789.1:p.Arg177=
ENST00000233838.9:c.1218C>G MANE Select	ENSP00000233838.3:p.Arg406=
ENST00000233838.8:c.1218C>G	ENSP00000233838.3:p.Arg406=
ENST00000430215.7:c.1047C>G	ENSP00000408045.3:p.Arg349=
ENST00000465637.5:n.179-5004C>G
ENST00000473665.1:n.711C>G
ENST00000482662.1:n.635C>G
NM_000821.5:c.1218C>G	NP_000812.2:p.Arg406=
NM_000821.6:c.1218C>G	NP_000812.2:p.Arg406=
NM_001142269.2:c.1047C>G	NP_001135741.1:p.Arg349=
NM_001142269.3:c.1047C>G	NP_001135741.1:p.Arg349=
XM_005264259.3:c.1218C>G	XP_005264316.1:p.Arg406=
XM_011532764.1:c.396C>G	XP_011531066.1:p.Arg132=
XM_011532765.1:c.396C>G	XP_011531067.1:p.Arg132=
XR_939677.1:n.1283C>G
XM_005264259.5:c.1218C>G	XP_005264316.1:p.Arg406=
XM_011532764.3:c.396C>G	XP_011531066.1:p.Arg132=
XM_011532765.3:c.396C>G	XP_011531067.1:p.Arg132=
XM_017003803.2:c.1047C>G	XP_016859292.1:p.Arg349=
XR_001738703.2:n.1283C>G
NM_000821.7:c.1218C>G MANE Select	NP_000812.2:p.Arg406=
NM_001142269.4:c.1047C>G	NP_001135741.1:p.Arg349=