Canonical Allele Identifier: CA1266821023
Gene: GGCX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.85546556_85546557delinsAC , CM000664.2:g.85546556_85546557delinsAC GRCh38
NC_000002.11:g.85773679_85773680delinsAC , CM000664.1:g.85773679_85773680delinsAC GRCh37
NC_000002.10:g.85627190_85627191delinsAC NCBI36
NG_011811.2:g.19978_19979delinsGT
NG_029183.1:g.12579_12580delinsAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000233838.9:c.*3377_*3378delinsGT MANE Select ENSP00000233838.3:n.*3377_*3378delinsGT
ENST00000233838.8:c.*3377_*3378delinsGT ENSP00000233838.3:n.*3377_*3378delinsGT
NM_000821.5:c.*3377_*3378delinsGT NP_000812.2:n.*3377_*3378delinsGT
NM_000821.6:c.*3377_*3378delinsGT NP_000812.2:n.*3377_*3378delinsGT
NM_001142269.2:c.*3377_*3378delinsGT NP_001135741.1:n.*3377_*3378delinsGT
NM_001142269.3:c.*3377_*3378delinsGT NP_001135741.1:n.*3377_*3378delinsGT
NM_000821.7:c.*3377_*3378delinsGT MANE Select NP_000812.2:n.*3377_*3378delinsGT
NM_001142269.4:c.*3377_*3378delinsGT NP_001135741.1:n.*3377_*3378delinsGT