Canonical Allele Identifier: CA1266821327
Gene: GGCX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.85546790_85546791delinsAC , CM000664.2:g.85546790_85546791delinsAC GRCh38
NC_000002.11:g.85773913_85773914delinsAC , CM000664.1:g.85773913_85773914delinsAC GRCh37
NC_000002.10:g.85627424_85627425delinsAC NCBI36
NG_011811.2:g.19744_19745delinsGT
NG_029183.1:g.12813_12814delinsAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000233838.9:c.*3143_*3144delinsGT MANE Select ENSP00000233838.3:n.*3143_*3144delinsGT
ENST00000233838.8:c.*3143_*3144delinsGT ENSP00000233838.3:n.*3143_*3144delinsGT
NM_000821.5:c.*3143_*3144delinsGT NP_000812.2:n.*3143_*3144delinsGT
NM_000821.6:c.*3143_*3144delinsGT NP_000812.2:n.*3143_*3144delinsGT
NM_001142269.2:c.*3143_*3144delinsGT NP_001135741.1:n.*3143_*3144delinsGT
NM_001142269.3:c.*3143_*3144delinsGT NP_001135741.1:n.*3143_*3144delinsGT
NM_000821.7:c.*3143_*3144delinsGT MANE Select NP_000812.2:n.*3143_*3144delinsGT
NM_001142269.4:c.*3143_*3144delinsGT NP_001135741.1:n.*3143_*3144delinsGT