Canonical Allele Identifier: CA1682451551
Gene: UNCX HGNC NCBI

Linked Data

dbSNP Id: rs1778694759

Genomic Alleles

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

Transcript Alleles

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