Canonical Allele Identifier: CA1682451617
Gene: UNCX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.1234145G= , CM000669.2:g.1234145G= GRCh38
NC_000007.13:g.1273781G= , CM000669.1:g.1273781G= GRCh37
NC_000007.12:g.1240307G= NCBI36

Transcript Alleles

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