Canonical Allele Identifier: CA1924448100
Gene: CDHR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.84203137_84203144delinsCCCCTCAG , CM000672.2:g.84203137_84203144delinsCCCCTCAG GRCh38
NC_000010.10:g.85962893_85962900delinsCCCCTCAG , CM000672.1:g.85962893_85962900delinsCCCCTCAG GRCh37
NC_000010.9:g.85952873_85952880delinsCCCCTCAG NCBI36
NG_028034.1:g.13482_13489delinsCCCCTCAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000623527.4:c.783+14_783+21delinsCCCCTCAG MANE Select ENSP00000485478.1:n.783+14_783+21delinsCCCCTCAG
ENST00000332904.7:c.783+14_783+21delinsCCCCTCAG ENSP00000331063.3:n.783+14_783+21delinsCCCCTCAG
ENST00000372117.6:c.163+14_163+21delinsCCCCTCAG
ENST00000623527.3:c.783+14_783+21delinsCCCCTCAG ENSP00000485478.1:n.783+14_783+21delinsCCCCTCAG
NM_001171971.2:c.783+14_783+21delinsCCCCTCAG NP_001165442.1:n.783+14_783+21delinsCCCCTCAG
NM_033100.3:c.783+14_783+21delinsCCCCTCAG NP_149091.1:n.783+14_783+21delinsCCCCTCAG
XM_011540337.1:c.957+14_957+21delinsCCCCTCAG XP_011538639.1:n.957+14_957+21delinsCCCCTCAG
XM_011540338.1:c.957+14_957+21delinsCCCCTCAG XP_011538640.1:n.957+14_957+21delinsCCCCTCAG
XM_011540339.1:c.404+14_404+21delinsCCCCTCAG XP_011538641.1:n.404+14_404+21delinsCCCCTCAG
XM_011540340.1:c.957+14_957+21delinsCCCCTCAG XP_011538642.1:n.957+14_957+21delinsCCCCTCAG
XM_011540340.3:c.957+14_957+21delinsCCCCTCAG XP_011538642.1:n.957+14_957+21delinsCCCCTCAG
NM_033100.4:c.783+14_783+21delinsCCCCTCAG MANE Select NP_149091.1:n.783+14_783+21delinsCCCCTCAG
NM_001171971.3:c.783+14_783+21delinsCCCCTCAG NP_001165442.1:n.783+14_783+21delinsCCCCTCAG