Canonical Allele Identifier: CA1682451679
Gene: UNCX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.1234271_1234272delinsGA , CM000669.2:g.1234271_1234272delinsGA GRCh38
NC_000007.13:g.1273907_1273908delinsGA , CM000669.1:g.1273907_1273908delinsGA GRCh37
NC_000007.12:g.1240433_1240434delinsGA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000316333.9:c.450+576_450+577delinsGA MANE Select ENSP00000314480.8:n.450+576_450+577delinsGA
ENST00000316333.8:c.450+576_450+577delinsGA ENSP00000314480.8:n.450+576_450+577delinsGA
NM_001080461.1:c.450+576_450+577delinsGA NP_001073930.1:n.450+576_450+577delinsGA
NM_001080461.2:c.450+576_450+577delinsGA NP_001073930.1:n.450+576_450+577delinsGA
NM_001080461.3:c.450+576_450+577delinsGA MANE Select NP_001073930.1:n.450+576_450+577delinsGA