Canonical Allele Identifier: CA1266819870
Gene: GGCX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.85545842_85545845delinsGAGA , CM000664.2:g.85545842_85545845delinsGAGA GRCh38
NC_000002.11:g.85772965_85772968delinsGAGA , CM000664.1:g.85772965_85772968delinsGAGA GRCh37
NC_000002.10:g.85626476_85626479delinsGAGA NCBI36
NG_011811.2:g.20690_20693delinsTCTC
NG_029183.1:g.11865_11868delinsGAGA

Transcript Alleles

HGVS Amino-acid change
ENST00000233838.9:c.*4089_*4092delinsTCTC MANE Select ENSP00000233838.3:n.*4089_*4092delinsTCTC...
ENST00000233838.8:c.*4089_*4092delinsTCTC ENSP00000233838.3:n.*4089_*4092delinsTCTC...
NM_000821.5:c.*4089_*4092delinsTCTC NP_000812.2:n.*4089_*4092delinsTCTC
NM_000821.6:c.*4089_*4092delinsTCTC NP_000812.2:n.*4089_*4092delinsTCTC
NM_001142269.2:c.*4089_*4092delinsTCTC NP_001135741.1:n.*4089_*4092delinsTCTC
NM_001142269.3:c.*4089_*4092delinsTCTC NP_001135741.1:n.*4089_*4092delinsTCTC
NM_000821.7:c.*4089_*4092delinsTCTC MANE Select NP_000812.2:n.*4089_*4092delinsTCTC
NM_001142269.4:c.*4089_*4092delinsTCTC NP_001135741.1:n.*4089_*4092delinsTCTC