Canonical Allele Identifier: CA2609953631

Gene: CDHR1

Linked Data

• gnomAD v4: 10-84203136-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.84203136C>T , CM000672.2:g.84203136C>T	GRCh38
NC_000010.10:g.85962892C>T , CM000672.1:g.85962892C>T	GRCh37
NC_000010.9:g.85952872C>T	NCBI36
NG_028034.1:g.13481C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000623527.4:c.783+13C>T MANE Select	ENSP00000485478.1:n.783+13C>T
ENST00000332904.7:c.783+13C>T	ENSP00000331063.3:n.783+13C>T
ENST00000372117.6:c.163+13C>T
ENST00000623527.3:c.783+13C>T	ENSP00000485478.1:n.783+13C>T
NM_001171971.2:c.783+13C>T	NP_001165442.1:n.783+13C>T
NM_033100.3:c.783+13C>T	NP_149091.1:n.783+13C>T
XM_011540337.1:c.957+13C>T	XP_011538639.1:n.957+13C>T
XM_011540338.1:c.957+13C>T	XP_011538640.1:n.957+13C>T
XM_011540339.1:c.404+13C>T	XP_011538641.1:n.404+13C>T
XM_011540340.1:c.957+13C>T	XP_011538642.1:n.957+13C>T
XM_011540340.3:c.957+13C>T	XP_011538642.1:n.957+13C>T
NM_033100.4:c.783+13C>T MANE Select	NP_149091.1:n.783+13C>T
NM_001171971.3:c.783+13C>T	NP_001165442.1:n.783+13C>T