Canonical Allele Identifier: CA1682451578
Gene: UNCX HGNC NCBI

Linked Data

dbSNP Id: rs1778696134
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.1234094_1234098del , CM000669.2:g.1234094_1234098del GRCh38
NC_000007.13:g.1273730_1273734del , CM000669.1:g.1273730_1273734del GRCh37
NC_000007.12:g.1240256_1240260del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000316333.9:c.450+399_450+403del MANE Select ENSP00000314480.8:n.450+399_450+403del
ENST00000316333.8:c.450+399_450+403del ENSP00000314480.8:n.450+399_450+403del
NM_001080461.1:c.450+399_450+403del NP_001073930.1:n.450+399_450+403del
NM_001080461.2:c.450+399_450+403del NP_001073930.1:n.450+399_450+403del
NM_001080461.3:c.450+399_450+403del MANE Select NP_001073930.1:n.450+399_450+403del
Search 100 bp 5'
Search 100 bp 3'