Canonical Allele Identifier: CA51729435
Gene: GGCX HGNC NCBI

Linked Data

dbSNP Id: rs1007299542

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.85546409_85546412del , CM000664.2:g.85546409_85546412del GRCh38
NC_000002.11:g.85773532_85773535del , CM000664.1:g.85773532_85773535del GRCh37
NC_000002.10:g.85627043_85627046del NCBI36
NG_011811.2:g.20126_20129del
NG_029183.1:g.12432_12435del

Transcript Alleles

HGVS Amino-acid change
ENST00000233838.9:c.*3525_*3528del MANE Select ENSP00000233838.3:n.*3525_*3528del
ENST00000233838.8:c.*3525_*3528del ENSP00000233838.3:n.*3525_*3528del
NM_000821.5:c.*3525_*3528del NP_000812.2:n.*3525_*3528del
NM_000821.6:c.*3525_*3528del NP_000812.2:n.*3525_*3528del
NM_001142269.2:c.*3525_*3528del NP_001135741.1:n.*3525_*3528del
NM_001142269.3:c.*3525_*3528del NP_001135741.1:n.*3525_*3528del
NM_000821.7:c.*3525_*3528del MANE Select NP_000812.2:n.*3525_*3528del
NM_001142269.4:c.*3525_*3528del NP_001135741.1:n.*3525_*3528del