Canonical Allele Identifier: CA2501627372
Gene: UNCX HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.1234041G>T , CM000669.2:g.1234041G>T GRCh38
NC_000007.13:g.1273677G>T , CM000669.1:g.1273677G>T GRCh37
NC_000007.12:g.1240203G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000316333.9:c.450+346G>T MANE Select ENSP00000314480.8:n.450+346G>T
ENST00000316333.8:c.450+346G>T ENSP00000314480.8:n.450+346G>T
NM_001080461.1:c.450+346G>T NP_001073930.1:n.450+346G>T
NM_001080461.2:c.450+346G>T NP_001073930.1:n.450+346G>T
NM_001080461.3:c.450+346G>T MANE Select NP_001073930.1:n.450+346G>T
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