Canonical Allele Identifier: CA1266825367
Gene: GGCX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.85552968T= , CM000664.2:g.85552968T= GRCh38
NC_000002.11:g.85780091T= , CM000664.1:g.85780091T= GRCh37
NC_000002.10:g.85633602T= NCBI36
NG_011811.2:g.13567A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000473665.2:n.5302A=
ENST00000482662.2:n.3709A=
ENST00000685865.1:n.1661A=
ENST00000687250.1:n.1361A=
ENST00000687995.1:n.1610A=
ENST00000688205.1:c.*851A= ENSP00000509673.1:n.*851A=
ENST00000688788.1:n.1497A=
ENST00000689276.1:c.1189A= ENSP00000510012.1:p.Thr397=
ENST00000689576.1:c.1258A= ENSP00000508712.1:p.Thr420=
ENST00000690108.1:c.*914A= ENSP00000510617.1:n.*914A=
ENST00000690468.1:c.979A= ENSP00000509078.1:p.Thr327=
ENST00000690595.1:c.583A= ENSP00000508979.1:p.Thr195=
ENST00000691348.1:c.1087A= ENSP00000509369.1:p.Thr363=
ENST00000691410.1:c.*835A= ENSP00000508479.1:n.*835A=
ENST00000693287.1:c.574A= ENSP00000510264.1:p.Thr192=
ENST00000693681.1:c.571A= ENSP00000510789.1:p.Thr191=
ENST00000233838.9:c.1258A= MANE Select ENSP00000233838.3:p.Thr420=
ENST00000233838.8:c.1258A= ENSP00000233838.3:p.Thr420=
ENST00000430215.7:c.1087A= ENSP00000408045.3:p.Thr363=
ENST00000465637.5:n.179-4964A=
ENST00000473665.1:n.751A=
ENST00000482662.1:n.675A=
NM_000821.5:c.1258A= NP_000812.2:p.Thr420=
NM_000821.6:c.1258A= NP_000812.2:p.Thr420=
NM_001142269.2:c.1087A= NP_001135741.1:p.Thr363=
NM_001142269.3:c.1087A= NP_001135741.1:p.Thr363=
XM_005264259.3:c.1258A= XP_005264316.1:p.Thr420=
XM_011532764.1:c.436A= XP_011531066.1:p.Thr146=
XM_011532765.1:c.436A= XP_011531067.1:p.Thr146=
XR_939677.1:n.1323A=
XM_005264259.5:c.1258A= XP_005264316.1:p.Thr420=
XM_011532764.3:c.436A= XP_011531066.1:p.Thr146=
XM_011532765.3:c.436A= XP_011531067.1:p.Thr146=
XM_017003803.2:c.1087A= XP_016859292.1:p.Thr363=
XR_001738703.2:n.1323A=
NM_000821.7:c.1258A= MANE Select NP_000812.2:p.Thr420=
NM_001142269.4:c.1087A= NP_001135741.1:p.Thr363=