Canonical Allele Identifier: CA1266820993
Gene: GGCX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.85546533_85546536delinsGAAA , CM000664.2:g.85546533_85546536delinsGAAA GRCh38
NC_000002.11:g.85773656_85773659delinsGAAA , CM000664.1:g.85773656_85773659delinsGAAA GRCh37
NC_000002.10:g.85627167_85627170delinsGAAA NCBI36
NG_011811.2:g.19999_20002delinsTTTC
NG_029183.1:g.12556_12559delinsGAAA

Transcript Alleles

HGVS Amino-acid change
ENST00000233838.9:c.*3398_*3401delinsTTTC MANE Select ENSP00000233838.3:n.*3398_*3401delinsTTTC...
ENST00000233838.8:c.*3398_*3401delinsTTTC ENSP00000233838.3:n.*3398_*3401delinsTTTC...
NM_000821.5:c.*3398_*3401delinsTTTC NP_000812.2:n.*3398_*3401delinsTTTC
NM_000821.6:c.*3398_*3401delinsTTTC NP_000812.2:n.*3398_*3401delinsTTTC
NM_001142269.2:c.*3398_*3401delinsTTTC NP_001135741.1:n.*3398_*3401delinsTTTC
NM_001142269.3:c.*3398_*3401delinsTTTC NP_001135741.1:n.*3398_*3401delinsTTTC
NM_000821.7:c.*3398_*3401delinsTTTC MANE Select NP_000812.2:n.*3398_*3401delinsTTTC
NM_001142269.4:c.*3398_*3401delinsTTTC NP_001135741.1:n.*3398_*3401delinsTTTC