Canonical Allele Identifier: CA210380851

Gene: CDHR1

Linked Data

• dbSNP Id: rs1034141463
• MyVariant Identifiers: chr10:g.85962891T>C (hg19) ; chr10:g.84203135T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.84203135T>C , CM000672.2:g.84203135T>C	GRCh38
NC_000010.10:g.85962891T>C , CM000672.1:g.85962891T>C	GRCh37
NC_000010.9:g.85952871T>C	NCBI36
NG_028034.1:g.13480T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000623527.4:c.783+12T>C MANE Select	ENSP00000485478.1:n.783+12T>C
ENST00000332904.7:c.783+12T>C	ENSP00000331063.3:n.783+12T>C
ENST00000372117.6:c.163+12T>C
ENST00000623527.3:c.783+12T>C	ENSP00000485478.1:n.783+12T>C
NM_001171971.2:c.783+12T>C	NP_001165442.1:n.783+12T>C
NM_033100.3:c.783+12T>C	NP_149091.1:n.783+12T>C
XM_011540337.1:c.957+12T>C	XP_011538639.1:n.957+12T>C
XM_011540338.1:c.957+12T>C	XP_011538640.1:n.957+12T>C
XM_011540339.1:c.404+12T>C	XP_011538641.1:n.404+12T>C
XM_011540340.1:c.957+12T>C	XP_011538642.1:n.957+12T>C
XM_011540340.3:c.957+12T>C	XP_011538642.1:n.957+12T>C
NM_033100.4:c.783+12T>C MANE Select	NP_149091.1:n.783+12T>C
NM_001171971.3:c.783+12T>C	NP_001165442.1:n.783+12T>C