Canonical Allele Identifier: CA5580251
Gene: CDHR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.84214514C>G , CM000672.2:g.84214514C>G GRCh38
NC_000010.10:g.85974270C>G , CM000672.1:g.85974270C>G GRCh37
NC_000010.9:g.85964250C>G NCBI36
NG_028034.1:g.24859C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000623527.4:c.2473C>G MANE Select ENSP00000485478.1:p.Pro825Ala
ENST00000332904.7:c.2040+1166C>G ENSP00000331063.3:n.2040+1166C>G
ENST00000372117.6:c.1688C>G
ENST00000459673.1:n.905C>G
ENST00000623399.1:c.211+1166C>G
ENST00000623527.3:c.2473C>G ENSP00000485478.1:p.Pro825Ala
NM_001171971.2:c.2040+1166C>G NP_001165442.1:n.2040+1166C>G
NM_033100.3:c.2473C>G NP_149091.1:p.Pro825Ala
XM_011540337.1:c.2647C>G XP_011538639.1:p.Pro883Ala
XM_011540338.1:c.2214+1166C>G XP_011538640.1:n.2214+1166C>G
XM_011540339.1:c.2026C>G XP_011538641.1:p.Pro676Ala
NM_033100.4:c.2473C>G MANE Select NP_149091.1:p.Pro825Ala
NM_001171971.3:c.2040+1166C>G NP_001165442.1:n.2040+1166C>G