Canonical Allele Identifier: CA1441586052

Gene: QDPR

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.17492169_17492170delinsCA , CM000666.2:g.17492169_17492170delinsCA	GRCh38
NC_000004.11:g.17493792_17493793delinsCA , CM000666.1:g.17493792_17493793delinsCA	GRCh37
NC_000004.10:g.17102890_17102891delinsCA	NCBI36
NG_008763.1:g.25065_25066delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706645.1:n.1592+62_1592+63delinsTG
ENST00000281243.10:c.545+62_545+63delinsTG MANE Select	ENSP00000281243.5:n.545+62_545+63delinsTG
ENST00000281243.9:c.545+62_545+63delinsTG	ENSP00000281243.5:n.545+62_545+63delinsTG
ENST00000428702.6:c.452+62_452+63delinsTG	ENSP00000390944.2:n.452+62_452+63delinsTG
ENST00000501943.6:n.282+62_282+63delinsTG
ENST00000505710.1:c.364-1425_364-1424delinsTG
ENST00000507439.5:c.437-1425_437-1424delinsTG	ENSP00000423227.1:n.437-1425_437-1424delinsTG
ENST00000508623.5:c.437-4934_437-4933delinsTG	ENSP00000426377.1:n.437-4934_437-4933delinsTG
ENST00000511609.1:n.277+62_277+63delinsTG
ENST00000513615.5:c.437-1425_437-1424delinsTG	ENSP00000422759.1:n.437-1425_437-1424delinsTG
ENST00000514300.1:c.*368-1425_*368-1424delinsTG	ENSP00000426039.1:n.*368-1425_*368-1424delinsTG
NM_000320.2:c.545+62_545+63delinsTG	NP_000311.2:n.545+62_545+63delinsTG
NM_001306140.1:c.452+62_452+63delinsTG	NP_001293069.1:n.452+62_452+63delinsTG
XR_241677.1:n.600-1425_600-1424delinsTG
NR_156494.1:n.617-1425_617-1424delinsTG
NM_000320.3:c.545+62_545+63delinsTG MANE Select	NP_000311.2:n.545+62_545+63delinsTG
NM_001306140.2:c.452+62_452+63delinsTG	NP_001293069.1:n.452+62_452+63delinsTG
NR_156494.2:n.473-1425_473-1424delinsTG