Canonical Allele Identifier: CA1033077638
Gene: GGCX HGNC NCBI

Linked Data

dbSNP Id: rs1691635824

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.85545845_85545847del , CM000664.2:g.85545845_85545847del GRCh38
NC_000002.11:g.85772968_85772970del , CM000664.1:g.85772968_85772970del GRCh37
NC_000002.10:g.85626479_85626481del NCBI36
NG_011811.2:g.20690_20692del
NG_029183.1:g.11868_11870del

Transcript Alleles

HGVS Amino-acid change
ENST00000233838.9:c.*4089_*4091del MANE Select ENSP00000233838.3:n.*4089_*4091del
ENST00000233838.8:c.*4089_*4091del ENSP00000233838.3:n.*4089_*4091del
NM_000821.5:c.*4089_*4091del NP_000812.2:n.*4089_*4091del
NM_000821.6:c.*4089_*4091del NP_000812.2:n.*4089_*4091del
NM_001142269.2:c.*4089_*4091del NP_001135741.1:n.*4089_*4091del
NM_001142269.3:c.*4089_*4091del NP_001135741.1:n.*4089_*4091del
NM_000821.7:c.*4089_*4091del MANE Select NP_000812.2:n.*4089_*4091del
NM_001142269.4:c.*4089_*4091del NP_001135741.1:n.*4089_*4091del