Canonical Allele Identifier: CA894034851
Gene: GGCX HGNC NCBI

Linked Data

dbSNP Id: rs11415157

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.85546420_85546425del , CM000664.2:g.85546420_85546425del GRCh38
NC_000002.11:g.85773543_85773548del , CM000664.1:g.85773543_85773548del GRCh37
NC_000002.10:g.85627054_85627059del NCBI36
NG_011811.2:g.20113_20118del
NG_029183.1:g.12443_12448del

Transcript Alleles

HGVS Amino-acid change
ENST00000233838.9:c.*3512_*3517del MANE Select ENSP00000233838.3:n.*3512_*3517del
ENST00000233838.8:c.*3512_*3517del ENSP00000233838.3:n.*3512_*3517del
NM_000821.5:c.*3512_*3517del NP_000812.2:n.*3512_*3517del
NM_000821.6:c.*3512_*3517del NP_000812.2:n.*3512_*3517del
NM_001142269.2:c.*3512_*3517del NP_001135741.1:n.*3512_*3517del
NM_001142269.3:c.*3512_*3517del NP_001135741.1:n.*3512_*3517del
NM_000821.7:c.*3512_*3517del MANE Select NP_000812.2:n.*3512_*3517del
NM_001142269.4:c.*3512_*3517del NP_001135741.1:n.*3512_*3517del