Canonical Allele Identifier: CA1682451715
Gene: UNCX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.1234320C= , CM000669.2:g.1234320C= GRCh38
NC_000007.13:g.1273956C= , CM000669.1:g.1273956C= GRCh37
NC_000007.12:g.1240482C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000316333.9:c.450+625C= MANE Select ENSP00000314480.8:n.450+625C=
ENST00000316333.8:c.450+625C= ENSP00000314480.8:n.450+625C=
NM_001080461.1:c.450+625C= NP_001073930.1:n.450+625C=
NM_001080461.2:c.450+625C= NP_001073930.1:n.450+625C=
NM_001080461.3:c.450+625C= MANE Select NP_001073930.1:n.450+625C=