Canonical Allele Identifier: CA1097509725
Gene: UNCX HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.1234105_1234106insCCC , CM000669.2:g.1234105_1234106insCCC GRCh38
NC_000007.13:g.1273741_1273742insCCC , CM000669.1:g.1273741_1273742insCCC GRCh37
NC_000007.12:g.1240267_1240268insCCC NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000316333.9:c.450+410_450+411insCCC MANE Select ENSP00000314480.8:n.450+410_450+411insCCC...
ENST00000316333.8:c.450+410_450+411insCCC ENSP00000314480.8:n.450+410_450+411insCCC...
NM_001080461.1:c.450+410_450+411insCCC NP_001073930.1:n.450+410_450+411insCCC
NM_001080461.2:c.450+410_450+411insCCC NP_001073930.1:n.450+410_450+411insCCC
NM_001080461.3:c.450+410_450+411insCCC MANE Select NP_001073930.1:n.450+410_450+411insCCC