Canonical Allele Identifier: CA1266821208
Gene: GGCX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.85546710_85546711delinsTG , CM000664.2:g.85546710_85546711delinsTG GRCh38
NC_000002.11:g.85773833_85773834delinsTG , CM000664.1:g.85773833_85773834delinsTG GRCh37
NC_000002.10:g.85627344_85627345delinsTG NCBI36
NG_011811.2:g.19824_19825delinsCA
NG_029183.1:g.12733_12734delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000233838.9:c.*3223_*3224delinsCA MANE Select ENSP00000233838.3:n.*3223_*3224delinsCA
ENST00000233838.8:c.*3223_*3224delinsCA ENSP00000233838.3:n.*3223_*3224delinsCA
NM_000821.5:c.*3223_*3224delinsCA NP_000812.2:n.*3223_*3224delinsCA
NM_000821.6:c.*3223_*3224delinsCA NP_000812.2:n.*3223_*3224delinsCA
NM_001142269.2:c.*3223_*3224delinsCA NP_001135741.1:n.*3223_*3224delinsCA
NM_001142269.3:c.*3223_*3224delinsCA NP_001135741.1:n.*3223_*3224delinsCA
NM_000821.7:c.*3223_*3224delinsCA MANE Select NP_000812.2:n.*3223_*3224delinsCA
NM_001142269.4:c.*3223_*3224delinsCA NP_001135741.1:n.*3223_*3224delinsCA