Canonical Allele Identifier: CA1266820800
Gene: GGCX HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.85546425_85546426delinsAG , CM000664.2:g.85546425_85546426delinsAG GRCh38
NC_000002.11:g.85773548_85773549delinsAG , CM000664.1:g.85773548_85773549delinsAG GRCh37
NC_000002.10:g.85627059_85627060delinsAG NCBI36
NG_011811.2:g.20109_20110delinsCT
NG_029183.1:g.12448_12449delinsAG

Transcript Alleles

HGVS Amino-acid change
ENST00000233838.9:c.*3508_*3509delinsCT MANE Select ENSP00000233838.3:n.*3508_*3509delinsCT
ENST00000233838.8:c.*3508_*3509delinsCT ENSP00000233838.3:n.*3508_*3509delinsCT
NM_000821.5:c.*3508_*3509delinsCT NP_000812.2:n.*3508_*3509delinsCT
NM_000821.6:c.*3508_*3509delinsCT NP_000812.2:n.*3508_*3509delinsCT
NM_001142269.2:c.*3508_*3509delinsCT NP_001135741.1:n.*3508_*3509delinsCT
NM_001142269.3:c.*3508_*3509delinsCT NP_001135741.1:n.*3508_*3509delinsCT
NM_000821.7:c.*3508_*3509delinsCT MANE Select NP_000812.2:n.*3508_*3509delinsCT
NM_001142269.4:c.*3508_*3509delinsCT NP_001135741.1:n.*3508_*3509delinsCT
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