Canonical Allele Identifier: CA2659852899
Gene: GGCX HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.85551953dup , CM000664.2:g.85551953dup GRCh38
NC_000002.11:g.85779076dup , CM000664.1:g.85779076dup GRCh37
NC_000002.10:g.85632587dup NCBI36
NG_011811.2:g.14582dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000473665.2:n.5946dup
ENST00000482662.2:n.4353dup
ENST00000685865.1:n.2305dup
ENST00000687250.1:n.2005dup
ENST00000687995.1:n.1820dup
ENST00000688205.1:c.*1061dup ENSP00000509673.1:n.*1061dup
ENST00000688788.1:n.1707dup
ENST00000689276.1:c.1399dup ENSP00000510012.1:p.Gln467ProfsTer?
ENST00000689576.1:c.*87dup ENSP00000508712.1:n.*87dup
ENST00000690108.1:c.*1124dup ENSP00000510617.1:n.*1124dup
ENST00000690468.1:c.*20dup ENSP00000509078.1:n.*20dup
ENST00000690595.1:c.793dup ENSP00000508979.1:p.Gln265ProfsTer?
ENST00000691348.1:c.*20dup ENSP00000509369.1:n.*20dup
ENST00000691410.1:c.*1045dup ENSP00000508479.1:n.*1045dup
ENST00000693287.1:c.784dup ENSP00000510264.1:p.Gln262ProfsTer?
ENST00000693681.1:c.781dup ENSP00000510789.1:p.Gln261ProfsTer?
ENST00000233838.9:c.1468dup MANE Select ENSP00000233838.3:p.Gln490ProfsTer?
ENST00000233838.8:c.1468dup ENSP00000233838.3:p.Gln490ProfsTer?
ENST00000430215.7:c.1297dup ENSP00000408045.3:p.Gln433ProfsTer?
ENST00000465637.5:n.179-3949dup
NM_000821.5:c.1468dup NP_000812.2:p.Gln490ProfsTer?
NM_000821.6:c.1468dup NP_000812.2:p.Gln490ProfsTer?
NM_001142269.2:c.1297dup NP_001135741.1:p.Gln433ProfsTer?
NM_001142269.3:c.1297dup NP_001135741.1:p.Gln433ProfsTer?
XM_005264259.3:c.1468dup XP_005264316.1:p.Gln490ProfsTer?
XM_011532764.1:c.646dup XP_011531066.1:p.Gln216ProfsTer?
XM_011532765.1:c.646dup XP_011531067.1:p.Gln216ProfsTer?
XR_939677.1:n.1381dup
XM_005264259.5:c.1468dup XP_005264316.1:p.Gln490ProfsTer?
XM_011532764.3:c.646dup XP_011531066.1:p.Gln216ProfsTer?
XM_011532765.3:c.646dup XP_011531067.1:p.Gln216ProfsTer?
XM_017003803.2:c.1297dup XP_016859292.1:p.Gln433ProfsTer?
XR_001738703.2:n.1381dup
NM_000821.7:c.1468dup MANE Select NP_000812.2:p.Gln490ProfsTer?
NM_001142269.4:c.1297dup NP_001135741.1:p.Gln433ProfsTer?