Canonical Allele Identifier: CA5580180
Community Standard Title: NM_033100.4(CDHR1):c.2229G>A (p.Arg743=)
Gene: CDHR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.84214270G>A , CM000672.2:g.84214270G>A GRCh38
NC_000010.10:g.85974026G>A , CM000672.1:g.85974026G>A GRCh37
NC_000010.9:g.85964006G>A NCBI36
NG_028034.1:g.24615G>A

Transcript Alleles

HGVS Amino-acid Change
NM_033100.4:c.2229G>A MANE Select NP_149091.1:p.Arg743=
ENST00000623527.4:c.2229G>A MANE Select ENSP00000485478.1:p.Arg743=
NM_001171971.2:c.2040+922G>A NP_001165442.1:n.2040+922G>A
NM_001171971.3:c.2040+922G>A NP_001165442.1:n.2040+922G>A
NM_033100.3:c.2229G>A NP_149091.1:p.Arg743=
ENST00000332904.7:c.2040+922G>A ENSP00000331063.3:n.2040+922G>A
ENST00000372117.6:c.1444G>A
ENST00000459673.1:n.661G>A
ENST00000623399.1:c.211+922G>A
ENST00000623527.3:c.2229G>A ENSP00000485478.1:p.Arg743=
XM_011540337.1:c.2403G>A XP_011538639.1:p.Arg801=
XM_011540338.1:c.2214+922G>A XP_011538640.1:n.2214+922G>A
XM_011540339.1:c.1782G>A XP_011538641.1:p.Arg594=