Canonical Allele Identifier: CA894034203
Gene: GGCX HGNC NCBI

Linked Data

dbSNP Id: rs1172059662

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.85545754_85545757del , CM000664.2:g.85545754_85545757del GRCh38
NC_000002.11:g.85772877_85772880del , CM000664.1:g.85772877_85772880del GRCh37
NC_000002.10:g.85626388_85626391del NCBI36
NG_011811.2:g.20782_20785del
NG_029183.1:g.11777_11780del

Transcript Alleles

HGVS Amino-acid Change
ENST00000233838.9:c.*4181_*4184del MANE Select ENSP00000233838.3:n.*4181_*4184del
ENST00000233838.8:c.*4181_*4184del ENSP00000233838.3:n.*4181_*4184del
NM_000821.5:c.*4181_*4184del NP_000812.2:n.*4181_*4184del
NM_000821.6:c.*4181_*4184del NP_000812.2:n.*4181_*4184del
NM_001142269.2:c.*4181_*4184del NP_001135741.1:n.*4181_*4184del
NM_001142269.3:c.*4181_*4184del NP_001135741.1:n.*4181_*4184del
NM_000821.7:c.*4181_*4184del MANE Select NP_000812.2:n.*4181_*4184del
NM_001142269.4:c.*4181_*4184del NP_001135741.1:n.*4181_*4184del