Canonical Allele Identifier: CA347485046
Gene: GGCX HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.85551961T>C , CM000664.2:g.85551961T>C GRCh38
NC_000002.11:g.85779084T>C , CM000664.1:g.85779084T>C GRCh37
NC_000002.10:g.85632595T>C NCBI36
NG_011811.2:g.14574A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000473665.2:n.5938A>G
ENST00000482662.2:n.4345A>G
ENST00000685865.1:n.2297A>G
ENST00000687250.1:n.1997A>G
ENST00000687995.1:n.1812A>G
ENST00000688205.1:c.*1053A>G ENSP00000509673.1:n.*1053A>G
ENST00000688788.1:n.1699A>G
ENST00000689276.1:c.1391A>G ENSP00000510012.1:p.Asp464Gly
ENST00000689576.1:c.*79A>G ENSP00000508712.1:n.*79A>G
ENST00000690108.1:c.*1116A>G ENSP00000510617.1:n.*1116A>G
ENST00000690468.1:c.*12A>G ENSP00000509078.1:n.*12A>G
ENST00000690595.1:c.785A>G ENSP00000508979.1:p.Asp262Gly
ENST00000691348.1:c.*12A>G ENSP00000509369.1:n.*12A>G
ENST00000691410.1:c.*1037A>G ENSP00000508479.1:n.*1037A>G
ENST00000693287.1:c.776A>G ENSP00000510264.1:p.Asp259Gly
ENST00000693681.1:c.773A>G ENSP00000510789.1:p.Asp258Gly
ENST00000233838.9:c.1460A>G MANE Select ENSP00000233838.3:p.Asp487Gly
ENST00000233838.8:c.1460A>G ENSP00000233838.3:p.Asp487Gly
ENST00000430215.7:c.1289A>G ENSP00000408045.3:p.Asp430Gly
ENST00000465637.5:n.179-3957A>G
NM_000821.5:c.1460A>G NP_000812.2:p.Asp487Gly
NM_000821.6:c.1460A>G NP_000812.2:p.Asp487Gly
NM_001142269.2:c.1289A>G NP_001135741.1:p.Asp430Gly
NM_001142269.3:c.1289A>G NP_001135741.1:p.Asp430Gly
XM_005264259.3:c.1460A>G XP_005264316.1:p.Asp487Gly
XM_011532764.1:c.638A>G XP_011531066.1:p.Asp213Gly
XM_011532765.1:c.638A>G XP_011531067.1:p.Asp213Gly
XR_939677.1:n.1373A>G
XM_005264259.5:c.1460A>G XP_005264316.1:p.Asp487Gly
XM_011532764.3:c.638A>G XP_011531066.1:p.Asp213Gly
XM_011532765.3:c.638A>G XP_011531067.1:p.Asp213Gly
XM_017003803.2:c.1289A>G XP_016859292.1:p.Asp430Gly
XR_001738703.2:n.1373A>G
NM_000821.7:c.1460A>G MANE Select NP_000812.2:p.Asp487Gly
NM_001142269.4:c.1289A>G NP_001135741.1:p.Asp430Gly