Canonical Allele Identifier: CA1097509614
Gene: UNCX HGNC NCBI

Linked Data

dbSNP Id: rs751327990

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.1234085_1234086insCCCCCCCCCCCC , CM000669.2:g.1234085_1234086insCCCCCCCCCCCC GRCh38
NC_000007.13:g.1273721_1273722insCCCCCCCCCCCC , CM000669.1:g.1273721_1273722insCCCCCCCCCCCC GRCh37
NC_000007.12:g.1240247_1240248insCCCCCCCCCCCC NCBI36

Transcript Alleles

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