Canonical Allele Identifier: CA1097509689
Gene: UNCX HGNC NCBI

Linked Data

gnomAD v3: 7-1234085-CG-C
gnomAD v4: 7-1234085-CG-C
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.1234086del , CM000669.2:g.1234086del GRCh38
NC_000007.13:g.1273722del , CM000669.1:g.1273722del GRCh37
NC_000007.12:g.1240248del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000316333.9:c.450+391del MANE Select ENSP00000314480.8:n.450+391del
ENST00000316333.8:c.450+391del ENSP00000314480.8:n.450+391del
NM_001080461.1:c.450+391del NP_001073930.1:n.450+391del
NM_001080461.2:c.450+391del NP_001073930.1:n.450+391del
NM_001080461.3:c.450+391del MANE Select NP_001073930.1:n.450+391del
Search 100 bp 5'
Search 100 bp 3'