Canonical Allele Identifier: CA1682451587
Gene: UNCX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.1234101_1234103delinsCAA , CM000669.2:g.1234101_1234103delinsCAA GRCh38
NC_000007.13:g.1273737_1273739delinsCAA , CM000669.1:g.1273737_1273739delinsCAA GRCh37
NC_000007.12:g.1240263_1240265delinsCAA NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000316333.9:c.450+406_450+408delinsCAA MANE Select ENSP00000314480.8:n.450+406_450+408delins...
ENST00000316333.8:c.450+406_450+408delinsCAA ENSP00000314480.8:n.450+406_450+408delins...
NM_001080461.1:c.450+406_450+408delinsCAA NP_001073930.1:n.450+406_450+408delinsCAA...
NM_001080461.2:c.450+406_450+408delinsCAA NP_001073930.1:n.450+406_450+408delinsCAA...
NM_001080461.3:c.450+406_450+408delinsCAA MANE Select NP_001073930.1:n.450+406_450+408delinsCAA...