Canonical Allele Identifier: CA1266824939
Gene: GGCX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.85551946G= , CM000664.2:g.85551946G= GRCh38
NC_000002.11:g.85779069G= , CM000664.1:g.85779069G= GRCh37
NC_000002.10:g.85632580G= NCBI36
NG_011811.2:g.14589C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000473665.2:n.5953C=
ENST00000482662.2:n.4360C=
ENST00000685865.1:n.2312C=
ENST00000687250.1:n.2012C=
ENST00000687995.1:n.1827C=
ENST00000688205.1:c.*1068C= ENSP00000509673.1:n.*1068C=
ENST00000688788.1:n.1714C=
ENST00000689276.1:c.1406C= ENSP00000510012.1:p.Ala469=
ENST00000689576.1:c.*94C= ENSP00000508712.1:n.*94C=
ENST00000690108.1:c.*1131C= ENSP00000510617.1:n.*1131C=
ENST00000690468.1:c.*27C= ENSP00000509078.1:n.*27C=
ENST00000690595.1:c.800C= ENSP00000508979.1:p.Ala267=
ENST00000691348.1:c.*27C= ENSP00000509369.1:n.*27C=
ENST00000691410.1:c.*1052C= ENSP00000508479.1:n.*1052C=
ENST00000693287.1:c.791C= ENSP00000510264.1:p.Ala264=
ENST00000693681.1:c.788C= ENSP00000510789.1:p.Ala263=
ENST00000233838.9:c.1475C= MANE Select ENSP00000233838.3:p.Ala492=
ENST00000233838.8:c.1475C= ENSP00000233838.3:p.Ala492=
ENST00000430215.7:c.1304C= ENSP00000408045.3:p.Ala435=
ENST00000465637.5:n.179-3942C=
NM_000821.5:c.1475C= NP_000812.2:p.Ala492=
NM_000821.6:c.1475C= NP_000812.2:p.Ala492=
NM_001142269.2:c.1304C= NP_001135741.1:p.Ala435=
NM_001142269.3:c.1304C= NP_001135741.1:p.Ala435=
XM_005264259.3:c.1475C= XP_005264316.1:p.Ala492=
XM_011532764.1:c.653C= XP_011531066.1:p.Ala218=
XM_011532765.1:c.653C= XP_011531067.1:p.Ala218=
XR_939677.1:n.1388C=
XM_005264259.5:c.1475C= XP_005264316.1:p.Ala492=
XM_011532764.3:c.653C= XP_011531066.1:p.Ala218=
XM_011532765.3:c.653C= XP_011531067.1:p.Ala218=
XM_017003803.2:c.1304C= XP_016859292.1:p.Ala435=
XR_001738703.2:n.1388C=
NM_000821.7:c.1475C= MANE Select NP_000812.2:p.Ala492=
NM_001142269.4:c.1304C= NP_001135741.1:p.Ala435=