Canonical Allele Identifier: CA2713552110
Gene: UNCX HGNC NCBI

Linked Data

dbSNP Id: rs1778694759

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.1234075_1234076insGGGGG , CM000669.2:g.1234075_1234076insGGGGG GRCh38
NC_000007.13:g.1273711_1273712insGGGGG , CM000669.1:g.1273711_1273712insGGGGG GRCh37
NC_000007.12:g.1240237_1240238insGGGGG NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000316333.9:c.450+380_450+381insGGGGG MANE Select ENSP00000314480.8:n.450+380_450+381insGGG...
ENST00000316333.8:c.450+380_450+381insGGGGG ENSP00000314480.8:n.450+380_450+381insGGG...
NM_001080461.1:c.450+380_450+381insGGGGG NP_001073930.1:n.450+380_450+381insGGGGG
NM_001080461.2:c.450+380_450+381insGGGGG NP_001073930.1:n.450+380_450+381insGGGGG
NM_001080461.3:c.450+380_450+381insGGGGG MANE Select NP_001073930.1:n.450+380_450+381insGGGGG