Canonical Allele Identifier: CA1266825392
Gene: GGCX HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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