Canonical Allele Identifier: CA1441586151
Gene: QDPR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.17492382_17492383delinsCA , CM000666.2:g.17492382_17492383delinsCA GRCh38
NC_000004.11:g.17494005_17494006delinsCA , CM000666.1:g.17494005_17494006delinsCA GRCh37
NC_000004.10:g.17103103_17103104delinsCA NCBI36
NG_008763.1:g.24852_24853delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000706645.1:n.1484-43_1484-42delinsTG
ENST00000281243.10:c.437-43_437-42delinsTG MANE Select ENSP00000281243.5:n.437-43_437-42delinsTG
ENST00000281243.9:c.437-43_437-42delinsTG ENSP00000281243.5:n.437-43_437-42delinsTG
ENST00000428702.6:c.344-43_344-42delinsTG ENSP00000390944.2:n.344-43_344-42delinsTG
ENST00000501943.6:n.131_132delinsTG
ENST00000505710.1:c.364-1638_364-1637delinsTG
ENST00000507439.5:c.437-1638_437-1637delinsTG ENSP00000423227.1:n.437-1638_437-1637delinsTG
ENST00000508623.5:c.437-5147_437-5146delinsTG ENSP00000426377.1:n.437-5147_437-5146delinsTG
ENST00000511609.1:n.126_127delinsTG
ENST00000513615.5:c.437-1638_437-1637delinsTG ENSP00000422759.1:n.437-1638_437-1637delinsTG
ENST00000514300.1:c.*368-1638_*368-1637delinsTG ENSP00000426039.1:n.*368-1638_*368-1637delinsTG
NM_000320.2:c.437-43_437-42delinsTG NP_000311.2:n.437-43_437-42delinsTG
NM_001306140.1:c.344-43_344-42delinsTG NP_001293069.1:n.344-43_344-42delinsTG
XR_241677.1:n.600-1638_600-1637delinsTG
NR_156494.1:n.617-1638_617-1637delinsTG
NM_000320.3:c.437-43_437-42delinsTG MANE Select NP_000311.2:n.437-43_437-42delinsTG
NM_001306140.2:c.344-43_344-42delinsTG NP_001293069.1:n.344-43_344-42delinsTG
NR_156494.2:n.473-1638_473-1637delinsTG