Canonical Allele Identifier: CA1266825568
Gene: GGCX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.85553413C= , CM000664.2:g.85553413C= GRCh38
NC_000002.11:g.85780536C= , CM000664.1:g.85780536C= GRCh37
NC_000002.10:g.85634047C= NCBI36
NG_011811.2:g.13122G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000473665.2:n.5018G=
ENST00000482662.2:n.3425G=
ENST00000685865.1:n.1377G=
ENST00000687250.1:n.1077G=
ENST00000687995.1:n.1326G=
ENST00000688205.1:c.*567G= ENSP00000509673.1:n.*567G=
ENST00000688788.1:n.1213G=
ENST00000689276.1:c.905G= ENSP00000510012.1:p.Arg302=
ENST00000689576.1:c.974G= ENSP00000508712.1:p.Arg325=
ENST00000690108.1:c.*630G= ENSP00000510617.1:n.*630G=
ENST00000690468.1:c.695G= ENSP00000509078.1:p.Arg232=
ENST00000690595.1:c.299G= ENSP00000508979.1:p.Arg100=
ENST00000691348.1:c.803G= ENSP00000509369.1:p.Arg268=
ENST00000691410.1:c.*551G= ENSP00000508479.1:n.*551G=
ENST00000693287.1:c.290G= ENSP00000510264.1:p.Arg97=
ENST00000693681.1:c.287G= ENSP00000510789.1:p.Arg96=
ENST00000233838.9:c.974G= MANE Select ENSP00000233838.3:p.Arg325=
ENST00000233838.8:c.974G= ENSP00000233838.3:p.Arg325=
ENST00000430215.7:c.803G= ENSP00000408045.3:p.Arg268=
ENST00000465637.5:n.179-5409G=
ENST00000473665.1:n.467G=
ENST00000482662.1:n.391G=
NM_000821.5:c.974G= NP_000812.2:p.Arg325=
NM_000821.6:c.974G= NP_000812.2:p.Arg325=
NM_001142269.2:c.803G= NP_001135741.1:p.Arg268=
NM_001142269.3:c.803G= NP_001135741.1:p.Arg268=
XM_005264259.3:c.974G= XP_005264316.1:p.Arg325=
XM_011532764.1:c.152G= XP_011531066.1:p.Arg51=
XM_011532765.1:c.152G= XP_011531067.1:p.Arg51=
XR_939677.1:n.1039G=
XM_005264259.5:c.974G= XP_005264316.1:p.Arg325=
XM_011532764.3:c.152G= XP_011531066.1:p.Arg51=
XM_011532765.3:c.152G= XP_011531067.1:p.Arg51=
XM_017003803.2:c.803G= XP_016859292.1:p.Arg268=
XR_001738703.2:n.1039G=
NM_000821.7:c.974G= MANE Select NP_000812.2:p.Arg325=
NM_001142269.4:c.803G= NP_001135741.1:p.Arg268=