Canonical Allele Identifier: CA1266824909
Gene: GGCX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.85551880G= , CM000664.2:g.85551880G= GRCh38
NC_000002.11:g.85779003G= , CM000664.1:g.85779003G= GRCh37
NC_000002.10:g.85632514G= NCBI36
NG_011811.2:g.14655C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000473665.2:n.6019C=
ENST00000482662.2:n.4426C=
ENST00000685865.1:n.2378C=
ENST00000687250.1:n.2078C=
ENST00000687995.1:n.1893C=
ENST00000688205.1:c.*1134C= ENSP00000509673.1:n.*1134C=
ENST00000688788.1:n.1780C=
ENST00000689276.1:c.1472C= ENSP00000510012.1:p.Ala491=
ENST00000689576.1:c.*160C= ENSP00000508712.1:n.*160C=
ENST00000690108.1:c.*1197C= ENSP00000510617.1:n.*1197C=
ENST00000690468.1:c.*93C= ENSP00000509078.1:n.*93C=
ENST00000690595.1:c.866C= ENSP00000508979.1:p.Ala289=
ENST00000691348.1:c.*93C= ENSP00000509369.1:n.*93C=
ENST00000691410.1:c.*1118C= ENSP00000508479.1:n.*1118C=
ENST00000693287.1:c.857C= ENSP00000510264.1:p.Ala286=
ENST00000693681.1:c.854C= ENSP00000510789.1:p.Ala285=
ENST00000233838.9:c.1541C= MANE Select ENSP00000233838.3:p.Ala514=
ENST00000233838.8:c.1541C= ENSP00000233838.3:p.Ala514=
ENST00000430215.7:c.1370C= ENSP00000408045.3:p.Ala457=
ENST00000465637.5:n.179-3876C=
NM_000821.5:c.1541C= NP_000812.2:p.Ala514=
NM_000821.6:c.1541C= NP_000812.2:p.Ala514=
NM_001142269.2:c.1370C= NP_001135741.1:p.Ala457=
NM_001142269.3:c.1370C= NP_001135741.1:p.Ala457=
XM_005264259.3:c.1541C= XP_005264316.1:p.Ala514=
XM_011532764.1:c.719C= XP_011531066.1:p.Ala240=
XM_011532765.1:c.719C= XP_011531067.1:p.Ala240=
XR_939677.1:n.1454C=
XM_005264259.5:c.1541C= XP_005264316.1:p.Ala514=
XM_011532764.3:c.719C= XP_011531066.1:p.Ala240=
XM_011532765.3:c.719C= XP_011531067.1:p.Ala240=
XM_017003803.2:c.1370C= XP_016859292.1:p.Ala457=
XR_001738703.2:n.1454C=
NM_000821.7:c.1541C= MANE Select NP_000812.2:p.Ala514=
NM_001142269.4:c.1370C= NP_001135741.1:p.Ala457=