Canonical Allele Identifier: CA1441585862

Gene: QDPR

Linked Data

• dbSNP Id: rs1718172725

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.17491794del , CM000666.2:g.17491794del	GRCh38
NC_000004.11:g.17493417del , CM000666.1:g.17493417del	GRCh37
NC_000004.10:g.17102515del	NCBI36
NG_008763.1:g.25441del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706645.1:n.1592+438del
ENST00000281243.10:c.545+438del MANE Select	ENSP00000281243.5:n.545+438del
ENST00000281243.9:c.545+438del	ENSP00000281243.5:n.545+438del
ENST00000428702.6:c.452+438del	ENSP00000390944.2:n.452+438del
ENST00000501943.6:n.282+438del
ENST00000505710.1:c.364-1049del
ENST00000507439.5:c.437-1049del	ENSP00000423227.1:n.437-1049del
ENST00000508623.5:c.437-4558del	ENSP00000426377.1:n.437-4558del
ENST00000511609.1:n.277+438del
ENST00000513615.5:c.437-1049del	ENSP00000422759.1:n.437-1049del
ENST00000514300.1:c.*368-1049del	ENSP00000426039.1:n.*368-1049del
NM_000320.2:c.545+438del	NP_000311.2:n.545+438del
NM_001306140.1:c.452+438del	NP_001293069.1:n.452+438del
XR_241677.1:n.600-1049del
NR_156494.1:n.617-1049del
NM_000320.3:c.545+438del MANE Select	NP_000311.2:n.545+438del
NM_001306140.2:c.452+438del	NP_001293069.1:n.452+438del
NR_156494.2:n.473-1049del