Canonical Allele Identifier: CA1266824953
Gene: GGCX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.85551976A= , CM000664.2:g.85551976A= GRCh38
NC_000002.11:g.85779099A= , CM000664.1:g.85779099A= GRCh37
NC_000002.10:g.85632610A= NCBI36
NG_011811.2:g.14559T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000473665.2:n.5923T=
ENST00000482662.2:n.4330T=
ENST00000685865.1:n.2282T=
ENST00000687250.1:n.1982T=
ENST00000687995.1:n.1797T=
ENST00000688205.1:c.*1038T= ENSP00000509673.1:n.*1038T=
ENST00000688788.1:n.1684T=
ENST00000689276.1:c.1376T= ENSP00000510012.1:p.Phe459=
ENST00000689576.1:c.*64T= ENSP00000508712.1:n.*64T=
ENST00000690108.1:c.*1101T= ENSP00000510617.1:n.*1101T=
ENST00000690468.1:c.1014T= ENSP00000509078.1:p.Phe338=
ENST00000690595.1:c.770T= ENSP00000508979.1:p.Phe257=
ENST00000691348.1:c.1122T= ENSP00000509369.1:p.Phe374=
ENST00000691410.1:c.*1022T= ENSP00000508479.1:n.*1022T=
ENST00000693287.1:c.761T= ENSP00000510264.1:p.Phe254=
ENST00000693681.1:c.758T= ENSP00000510789.1:p.Phe253=
ENST00000233838.9:c.1445T= MANE Select ENSP00000233838.3:p.Phe482=
ENST00000233838.8:c.1445T= ENSP00000233838.3:p.Phe482=
ENST00000430215.7:c.1274T= ENSP00000408045.3:p.Phe425=
ENST00000465637.5:n.179-3972T=
NM_000821.5:c.1445T= NP_000812.2:p.Phe482=
NM_000821.6:c.1445T= NP_000812.2:p.Phe482=
NM_001142269.2:c.1274T= NP_001135741.1:p.Phe425=
NM_001142269.3:c.1274T= NP_001135741.1:p.Phe425=
XM_005264259.3:c.1445T= XP_005264316.1:p.Phe482=
XM_011532764.1:c.623T= XP_011531066.1:p.Phe208=
XM_011532765.1:c.623T= XP_011531067.1:p.Phe208=
XR_939677.1:n.1358T=
XM_005264259.5:c.1445T= XP_005264316.1:p.Phe482=
XM_011532764.3:c.623T= XP_011531066.1:p.Phe208=
XM_011532765.3:c.623T= XP_011531067.1:p.Phe208=
XM_017003803.2:c.1274T= XP_016859292.1:p.Phe425=
XR_001738703.2:n.1358T=
NM_000821.7:c.1445T= MANE Select NP_000812.2:p.Phe482=
NM_001142269.4:c.1274T= NP_001135741.1:p.Phe425=