Canonical Allele Identifier: CA1441586029
Gene: QDPR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.17492137_17492138delinsAC , CM000666.2:g.17492137_17492138delinsAC GRCh38
NC_000004.11:g.17493760_17493761delinsAC , CM000666.1:g.17493760_17493761delinsAC GRCh37
NC_000004.10:g.17102858_17102859delinsAC NCBI36
NG_008763.1:g.25097_25098delinsGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000706645.1:n.1592+94_1592+95delinsGT
ENST00000281243.10:c.545+94_545+95delinsGT MANE Select ENSP00000281243.5:n.545+94_545+95delinsGT
ENST00000281243.9:c.545+94_545+95delinsGT ENSP00000281243.5:n.545+94_545+95delinsGT
ENST00000428702.6:c.452+94_452+95delinsGT ENSP00000390944.2:n.452+94_452+95delinsGT
ENST00000501943.6:n.282+94_282+95delinsGT
ENST00000505710.1:c.364-1393_364-1392delinsGT
ENST00000507439.5:c.437-1393_437-1392delinsGT ENSP00000423227.1:n.437-1393_437-1392delinsGT
ENST00000508623.5:c.437-4902_437-4901delinsGT ENSP00000426377.1:n.437-4902_437-4901delinsGT
ENST00000511609.1:n.277+94_277+95delinsGT
ENST00000513615.5:c.437-1393_437-1392delinsGT ENSP00000422759.1:n.437-1393_437-1392delinsGT
ENST00000514300.1:c.*368-1393_*368-1392delinsGT ENSP00000426039.1:n.*368-1393_*368-1392delinsGT
NM_000320.2:c.545+94_545+95delinsGT NP_000311.2:n.545+94_545+95delinsGT
NM_001306140.1:c.452+94_452+95delinsGT NP_001293069.1:n.452+94_452+95delinsGT
XR_241677.1:n.600-1393_600-1392delinsGT
NR_156494.1:n.617-1393_617-1392delinsGT
NM_000320.3:c.545+94_545+95delinsGT MANE Select NP_000311.2:n.545+94_545+95delinsGT
NM_001306140.2:c.452+94_452+95delinsGT NP_001293069.1:n.452+94_452+95delinsGT
NR_156494.2:n.473-1393_473-1392delinsGT