Canonical Allele Identifier: CA1441585920
Gene: QDPR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.17491917_17491919delinsCAT , CM000666.2:g.17491917_17491919delinsCAT GRCh38
NC_000004.11:g.17493540_17493542delinsCAT , CM000666.1:g.17493540_17493542delinsCAT GRCh37
NC_000004.10:g.17102638_17102640delinsCAT NCBI36
NG_008763.1:g.25316_25318delinsATG

Transcript Alleles

HGVS Amino-acid Change
ENST00000706645.1:n.1592+313_1592+315delinsATG
ENST00000281243.10:c.545+313_545+315delinsATG MANE Select ENSP00000281243.5:n.545+313_545+315delinsATG
ENST00000281243.9:c.545+313_545+315delinsATG ENSP00000281243.5:n.545+313_545+315delinsATG
ENST00000428702.6:c.452+313_452+315delinsATG ENSP00000390944.2:n.452+313_452+315delinsATG
ENST00000501943.6:n.282+313_282+315delinsATG
ENST00000505710.1:c.364-1174_364-1172delinsATG
ENST00000507439.5:c.437-1174_437-1172delinsATG ENSP00000423227.1:n.437-1174_437-1172delinsATG
ENST00000508623.5:c.437-4683_437-4681delinsATG ENSP00000426377.1:n.437-4683_437-4681delinsATG
ENST00000511609.1:n.277+313_277+315delinsATG
ENST00000513615.5:c.437-1174_437-1172delinsATG ENSP00000422759.1:n.437-1174_437-1172delinsATG
ENST00000514300.1:c.*368-1174_*368-1172delinsATG ENSP00000426039.1:n.*368-1174_*368-1172delinsATG
NM_000320.2:c.545+313_545+315delinsATG NP_000311.2:n.545+313_545+315delinsATG
NM_001306140.1:c.452+313_452+315delinsATG NP_001293069.1:n.452+313_452+315delinsATG
XR_241677.1:n.600-1174_600-1172delinsATG
NR_156494.1:n.617-1174_617-1172delinsATG
NM_000320.3:c.545+313_545+315delinsATG MANE Select NP_000311.2:n.545+313_545+315delinsATG
NM_001306140.2:c.452+313_452+315delinsATG NP_001293069.1:n.452+313_452+315delinsATG
NR_156494.2:n.473-1174_473-1172delinsATG