Canonical Allele Identifier: CA2609953636

Gene: CDHR1

Linked Data

• gnomAD v4: 10-84203144-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.84203144G>A , CM000672.2:g.84203144G>A	GRCh38
NC_000010.10:g.85962900G>A , CM000672.1:g.85962900G>A	GRCh37
NC_000010.9:g.85952880G>A	NCBI36
NG_028034.1:g.13489G>A

Transcript Alleles

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