Canonical Allele Identifier: CA377379476
Community Standard Title: NM_033100.4(CDHR1):c.2197G>T (p.Val733Phe)
Gene: CDHR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.84214238G>T , CM000672.2:g.84214238G>T GRCh38
NC_000010.10:g.85973994G>T , CM000672.1:g.85973994G>T GRCh37
NC_000010.9:g.85963974G>T NCBI36
NG_028034.1:g.24583G>T

Transcript Alleles

HGVS Amino-acid Change
NM_033100.4:c.2197G>T MANE Select NP_149091.1:p.Val733Phe
ENST00000623527.4:c.2197G>T MANE Select ENSP00000485478.1:p.Val733Phe
NM_001171971.2:c.2040+890G>T NP_001165442.1:n.2040+890G>T
NM_001171971.3:c.2040+890G>T NP_001165442.1:n.2040+890G>T
NM_033100.3:c.2197G>T NP_149091.1:p.Val733Phe
ENST00000332904.7:c.2040+890G>T ENSP00000331063.3:n.2040+890G>T
ENST00000372117.6:c.1412G>T
ENST00000459673.1:n.629G>T
ENST00000623399.1:c.211+890G>T
ENST00000623527.3:c.2197G>T ENSP00000485478.1:p.Val733Phe
XM_011540337.1:c.2371G>T XP_011538639.1:p.Val791Phe
XM_011540338.1:c.2214+890G>T XP_011538640.1:n.2214+890G>T
XM_011540339.1:c.1750G>T XP_011538641.1:p.Val584Phe