Canonical Allele Identifier: CA1266820658
Gene: GGCX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.85546380_85546390delinsGCCACCACACT , CM000664.2:g.85546380_85546390delinsGCCACCACACT GRCh38
NC_000002.11:g.85773503_85773513delinsGCCACCACACT , CM000664.1:g.85773503_85773513delinsGCCACCACACT GRCh37
NC_000002.10:g.85627014_85627024delinsGCCACCACACT NCBI36
NG_011811.2:g.20145_20155delinsAGTGTGGTGGC
NG_029183.1:g.12403_12413delinsGCCACCACACT

Transcript Alleles

HGVS Amino-acid Change
ENST00000233838.9:c.*3544_*3554delinsAGTGTGGTGGC MANE Select ENSP00000233838.3:n.*3544_*3554delinsAGTGTGGTGGC
ENST00000233838.8:c.*3544_*3554delinsAGTGTGGTGGC ENSP00000233838.3:n.*3544_*3554delinsAGTGTGGTGGC
NM_000821.5:c.*3544_*3554delinsAGTGTGGTGGC NP_000812.2:n.*3544_*3554delinsAGTGTGGTGGC
NM_000821.6:c.*3544_*3554delinsAGTGTGGTGGC NP_000812.2:n.*3544_*3554delinsAGTGTGGTGGC
NM_001142269.2:c.*3544_*3554delinsAGTGTGGTGGC NP_001135741.1:n.*3544_*3554delinsAGTGTGGTGGC
NM_001142269.3:c.*3544_*3554delinsAGTGTGGTGGC NP_001135741.1:n.*3544_*3554delinsAGTGTGGTGGC
NM_000821.7:c.*3544_*3554delinsAGTGTGGTGGC MANE Select NP_000812.2:n.*3544_*3554delinsAGTGTGGTGGC
NM_001142269.4:c.*3544_*3554delinsAGTGTGGTGGC NP_001135741.1:n.*3544_*3554delinsAGTGTGGTGGC