Canonical Allele Identifier: CA1682451698
Gene: UNCX HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.1234297A= , CM000669.2:g.1234297A= GRCh38
NC_000007.13:g.1273933A= , CM000669.1:g.1273933A= GRCh37
NC_000007.12:g.1240459A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000316333.9:c.450+602A= MANE Select ENSP00000314480.8:n.450+602A=
ENST00000316333.8:c.450+602A= ENSP00000314480.8:n.450+602A=
NM_001080461.1:c.450+602A= NP_001073930.1:n.450+602A=
NM_001080461.2:c.450+602A= NP_001073930.1:n.450+602A=
NM_001080461.3:c.450+602A= MANE Select NP_001073930.1:n.450+602A=
Search 100 bp 5'
Search 100 bp 3'