Canonical Allele Identifier: CA1682451636
Gene: UNCX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.1234165_1234166delinsCA , CM000669.2:g.1234165_1234166delinsCA GRCh38
NC_000007.13:g.1273801_1273802delinsCA , CM000669.1:g.1273801_1273802delinsCA GRCh37
NC_000007.12:g.1240327_1240328delinsCA NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000316333.9:c.450+470_450+471delinsCA MANE Select ENSP00000314480.8:n.450+470_450+471delins...
ENST00000316333.8:c.450+470_450+471delinsCA ENSP00000314480.8:n.450+470_450+471delins...
NM_001080461.1:c.450+470_450+471delinsCA NP_001073930.1:n.450+470_450+471delinsCA
NM_001080461.2:c.450+470_450+471delinsCA NP_001073930.1:n.450+470_450+471delinsCA
NM_001080461.3:c.450+470_450+471delinsCA MANE Select NP_001073930.1:n.450+470_450+471delinsCA