Canonical Allele Identifier: CA1097509623
Gene: UNCX HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.1234085_1234086insCCCCCCCCCACCCCCCCC , CM000669.2:g.1234085_1234086insCCCCCCCCCACCCCCCCC GRCh38
NC_000007.13:g.1273721_1273722insCCCCCCCCCACCCCCCCC , CM000669.1:g.1273721_1273722insCCCCCCCCCACCCCCCCC GRCh37
NC_000007.12:g.1240247_1240248insCCCCCCCCCACCCCCCCC NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000316333.9:c.450+390_450+391insCCCCCCCCCACCCCCCCC MANE Select ENSP00000314480.8:n.450+390_450+391insCCC...
ENST00000316333.8:c.450+390_450+391insCCCCCCCCCACCCCCCCC ENSP00000314480.8:n.450+390_450+391insCCC...
NM_001080461.1:c.450+390_450+391insCCCCCCCCCACCCCCCCC NP_001073930.1:n.450+390_450+391insCCCCCC...
NM_001080461.2:c.450+390_450+391insCCCCCCCCCACCCCCCCC NP_001073930.1:n.450+390_450+391insCCCCCC...
NM_001080461.3:c.450+390_450+391insCCCCCCCCCACCCCCCCC MANE Select NP_001073930.1:n.450+390_450+391insCCCCCC...