Canonical Allele Identifier: CA1033078029
Gene: GGCX HGNC NCBI

Linked Data

dbSNP Id: rs1691667679

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.85546404_85546405del , CM000664.2:g.85546404_85546405del GRCh38
NC_000002.11:g.85773527_85773528del , CM000664.1:g.85773527_85773528del GRCh37
NC_000002.10:g.85627038_85627039del NCBI36
NG_011811.2:g.20131_20132del
NG_029183.1:g.12427_12428del

Transcript Alleles

HGVS Amino-acid change
ENST00000233838.9:c.*3530_*3531del MANE Select ENSP00000233838.3:n.*3530_*3531del
ENST00000233838.8:c.*3530_*3531del ENSP00000233838.3:n.*3530_*3531del
NM_000821.5:c.*3530_*3531del NP_000812.2:n.*3530_*3531del
NM_000821.6:c.*3530_*3531del NP_000812.2:n.*3530_*3531del
NM_001142269.2:c.*3530_*3531del NP_001135741.1:n.*3530_*3531del
NM_001142269.3:c.*3530_*3531del NP_001135741.1:n.*3530_*3531del
NM_000821.7:c.*3530_*3531del MANE Select NP_000812.2:n.*3530_*3531del
NM_001142269.4:c.*3530_*3531del NP_001135741.1:n.*3530_*3531del