Canonical Allele Identifier: CA2670124630
Gene: QDPR HGNC NCBI

Linked Data

gnomAD v4: 4-17492605-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.17492605G>A , CM000666.2:g.17492605G>A GRCh38
NC_000004.11:g.17494228G>A , CM000666.1:g.17494228G>A GRCh37
NC_000004.10:g.17103326G>A NCBI36
NG_008763.1:g.24630C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000706645.1:n.1484-265C>T
ENST00000281243.10:c.437-265C>T MANE Select ENSP00000281243.5:n.437-265C>T
ENST00000281243.9:c.437-265C>T ENSP00000281243.5:n.437-265C>T
ENST00000428702.6:c.344-265C>T ENSP00000390944.2:n.344-265C>T
ENST00000505710.1:c.364-1860C>T
ENST00000507439.5:c.437-1860C>T ENSP00000423227.1:n.437-1860C>T
ENST00000508623.5:c.437-5369C>T ENSP00000426377.1:n.437-5369C>T
ENST00000513615.5:c.437-1860C>T ENSP00000422759.1:n.437-1860C>T
ENST00000514300.1:c.*368-1860C>T ENSP00000426039.1:n.*368-1860C>T
NM_000320.2:c.437-265C>T NP_000311.2:n.437-265C>T
NM_001306140.1:c.344-265C>T NP_001293069.1:n.344-265C>T
XR_241677.1:n.600-1860C>T
NR_156494.1:n.617-1860C>T
NM_000320.3:c.437-265C>T MANE Select NP_000311.2:n.437-265C>T
NM_001306140.2:c.344-265C>T NP_001293069.1:n.344-265C>T
NR_156494.2:n.473-1860C>T