Canonical Allele Identifier: CA2834866940
Gene: UNCX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.1234128del , CM000669.2:g.1234128del GRCh38
NC_000007.13:g.1273764del , CM000669.1:g.1273764del GRCh37
NC_000007.12:g.1240290del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000316333.9:c.450+433del MANE Select ENSP00000314480.8:n.450+433del
ENST00000316333.8:c.450+433del ENSP00000314480.8:n.450+433del
NM_001080461.1:c.450+433del NP_001073930.1:n.450+433del
NM_001080461.2:c.450+433del NP_001073930.1:n.450+433del
NM_001080461.3:c.450+433del MANE Select NP_001073930.1:n.450+433del