Canonical Allele Identifier: CA1266819922
Gene: GGCX HGNC NCBI

Linked Data

dbSNP Id: rs1691638523
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.85545888_85545891del , CM000664.2:g.85545888_85545891del GRCh38
NC_000002.11:g.85773011_85773014del , CM000664.1:g.85773011_85773014del GRCh37
NC_000002.10:g.85626522_85626525del NCBI36
NG_011811.2:g.20648_20651del
NG_029183.1:g.11911_11914del

Transcript Alleles

HGVS Amino-acid change
ENST00000233838.9:c.*4047_*4050del MANE Select ENSP00000233838.3:n.*4047_*4050del
ENST00000233838.8:c.*4047_*4050del ENSP00000233838.3:n.*4047_*4050del
NM_000821.5:c.*4047_*4050del NP_000812.2:n.*4047_*4050del
NM_000821.6:c.*4047_*4050del NP_000812.2:n.*4047_*4050del
NM_001142269.2:c.*4047_*4050del NP_001135741.1:n.*4047_*4050del
NM_001142269.3:c.*4047_*4050del NP_001135741.1:n.*4047_*4050del
NM_000821.7:c.*4047_*4050del MANE Select NP_000812.2:n.*4047_*4050del
NM_001142269.4:c.*4047_*4050del NP_001135741.1:n.*4047_*4050del
Search 100 bp 5'
Search 100 bp 3'