Canonical Allele Identifier: CA1266821499
Gene: GGCX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.85546950_85546951delinsCA , CM000664.2:g.85546950_85546951delinsCA GRCh38
NC_000002.11:g.85774073_85774074delinsCA , CM000664.1:g.85774073_85774074delinsCA GRCh37
NC_000002.10:g.85627584_85627585delinsCA NCBI36
NG_011811.2:g.19584_19585delinsTG
NG_029183.1:g.12973_12974delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000233838.9:c.*2983_*2984delinsTG MANE Select ENSP00000233838.3:n.*2983_*2984delinsTG
ENST00000233838.8:c.*2983_*2984delinsTG ENSP00000233838.3:n.*2983_*2984delinsTG
NM_000821.5:c.*2983_*2984delinsTG NP_000812.2:n.*2983_*2984delinsTG
NM_000821.6:c.*2983_*2984delinsTG NP_000812.2:n.*2983_*2984delinsTG
NM_001142269.2:c.*2983_*2984delinsTG NP_001135741.1:n.*2983_*2984delinsTG
NM_001142269.3:c.*2983_*2984delinsTG NP_001135741.1:n.*2983_*2984delinsTG
NM_000821.7:c.*2983_*2984delinsTG MANE Select NP_000812.2:n.*2983_*2984delinsTG
NM_001142269.4:c.*2983_*2984delinsTG NP_001135741.1:n.*2983_*2984delinsTG