Canonical Allele Identifier: CA1682451622
Gene: UNCX HGNC NCBI

Linked Data

dbSNP Id: rs1778697597
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.1234147_1234148del , CM000669.2:g.1234147_1234148del GRCh38
NC_000007.13:g.1273783_1273784del , CM000669.1:g.1273783_1273784del GRCh37
NC_000007.12:g.1240309_1240310del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000316333.9:c.450+452_450+453del MANE Select ENSP00000314480.8:n.450+452_450+453del
ENST00000316333.8:c.450+452_450+453del ENSP00000314480.8:n.450+452_450+453del
NM_001080461.1:c.450+452_450+453del NP_001073930.1:n.450+452_450+453del
NM_001080461.2:c.450+452_450+453del NP_001073930.1:n.450+452_450+453del
NM_001080461.3:c.450+452_450+453del MANE Select NP_001073930.1:n.450+452_450+453del
Search 100 bp 5'
Search 100 bp 3'