Canonical Allele Identifier: CA1441585866

Gene: QDPR

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.17491803_17491807delinsAATAG , CM000666.2:g.17491803_17491807delinsAATAG	GRCh38
NC_000004.11:g.17493426_17493430delinsAATAG , CM000666.1:g.17493426_17493430delinsAATAG	GRCh37
NC_000004.10:g.17102524_17102528delinsAATAG	NCBI36
NG_008763.1:g.25428_25432delinsCTATT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706645.1:n.1592+425_1592+429delinsCTATT
ENST00000281243.10:c.545+425_545+429delinsCTATT MANE Select	ENSP00000281243.5:n.545+425_545+429delinsCTATT
ENST00000281243.9:c.545+425_545+429delinsCTATT	ENSP00000281243.5:n.545+425_545+429delinsCTATT
ENST00000428702.6:c.452+425_452+429delinsCTATT	ENSP00000390944.2:n.452+425_452+429delinsCTATT
ENST00000501943.6:n.282+425_282+429delinsCTATT
ENST00000505710.1:c.364-1062_364-1058delinsCTATT
ENST00000507439.5:c.437-1062_437-1058delinsCTATT	ENSP00000423227.1:n.437-1062_437-1058delinsCTATT
ENST00000508623.5:c.437-4571_437-4567delinsCTATT	ENSP00000426377.1:n.437-4571_437-4567delinsCTATT
ENST00000511609.1:n.277+425_277+429delinsCTATT
ENST00000513615.5:c.437-1062_437-1058delinsCTATT	ENSP00000422759.1:n.437-1062_437-1058delinsCTATT
ENST00000514300.1:c.*368-1062_*368-1058delinsCTATT	ENSP00000426039.1:n.*368-1062_*368-1058delinsCTATT
NM_000320.2:c.545+425_545+429delinsCTATT	NP_000311.2:n.545+425_545+429delinsCTATT
NM_001306140.1:c.452+425_452+429delinsCTATT	NP_001293069.1:n.452+425_452+429delinsCTATT
XR_241677.1:n.600-1062_600-1058delinsCTATT
NR_156494.1:n.617-1062_617-1058delinsCTATT
NM_000320.3:c.545+425_545+429delinsCTATT MANE Select	NP_000311.2:n.545+425_545+429delinsCTATT
NM_001306140.2:c.452+425_452+429delinsCTATT	NP_001293069.1:n.452+425_452+429delinsCTATT
NR_156494.2:n.473-1062_473-1058delinsCTATT