Canonical Allele Identifier: CA1033078043
Gene: GGCX HGNC NCBI

Linked Data

dbSNP Id: rs1691668883

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.85546415_85546416del , CM000664.2:g.85546415_85546416del GRCh38
NC_000002.11:g.85773538_85773539del , CM000664.1:g.85773538_85773539del GRCh37
NC_000002.10:g.85627049_85627050del NCBI36
NG_011811.2:g.20119_20120del
NG_029183.1:g.12438_12439del

Transcript Alleles

HGVS Amino-acid change
ENST00000233838.9:c.*3518_*3519del MANE Select ENSP00000233838.3:n.*3518_*3519del
ENST00000233838.8:c.*3518_*3519del ENSP00000233838.3:n.*3518_*3519del
NM_000821.5:c.*3518_*3519del NP_000812.2:n.*3518_*3519del
NM_000821.6:c.*3518_*3519del NP_000812.2:n.*3518_*3519del
NM_001142269.2:c.*3518_*3519del NP_001135741.1:n.*3518_*3519del
NM_001142269.3:c.*3518_*3519del NP_001135741.1:n.*3518_*3519del
NM_000821.7:c.*3518_*3519del MANE Select NP_000812.2:n.*3518_*3519del
NM_001142269.4:c.*3518_*3519del NP_001135741.1:n.*3518_*3519del