Canonical Allele Identifier: CA1266819785
Gene: GGCX HGNC NCBI

Linked Data

dbSNP Id: rs1691629678
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.85545759dup , CM000664.2:g.85545759dup GRCh38
NC_000002.11:g.85772882dup , CM000664.1:g.85772882dup GRCh37
NC_000002.10:g.85626393dup NCBI36
NG_011811.2:g.20778dup
NG_029183.1:g.11782dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000233838.9:c.*4177dup MANE Select ENSP00000233838.3:n.*4177dup
ENST00000233838.8:c.*4177dup ENSP00000233838.3:n.*4177dup
NM_000821.5:c.*4177dup NP_000812.2:n.*4177dup
NM_000821.6:c.*4177dup NP_000812.2:n.*4177dup
NM_001142269.2:c.*4177dup NP_001135741.1:n.*4177dup
NM_001142269.3:c.*4177dup NP_001135741.1:n.*4177dup
NM_000821.7:c.*4177dup MANE Select NP_000812.2:n.*4177dup
NM_001142269.4:c.*4177dup NP_001135741.1:n.*4177dup
Search 100 bp 5'
Search 100 bp 3'