Canonical Allele Identifier: CA1441595149
Gene: QDPR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.17511992A= , CM000666.2:g.17511992A= GRCh38
NC_000004.11:g.17513615A= , CM000666.1:g.17513615A= GRCh37
NC_000004.10:g.17122713A= NCBI36
NG_008763.1:g.5243T=

Transcript Alleles

HGVS Amino-acid change
ENST00000281243.10:c.63T= MANE Select ENSP00000281243.5:p.Ala21=
ENST00000281243.9:c.63T= ENSP00000281243.5:p.Ala21=
ENST00000428702.6:c.63T= ENSP00000390944.2:p.Ala21=
ENST00000507439.5:c.63T= ENSP00000423227.1:p.Ala21=
ENST00000508623.5:c.63T= ENSP00000426377.1:p.Ala21=
ENST00000513615.5:c.63T= ENSP00000422759.1:p.Ala21=
ENST00000514300.1:c.63T= ENSP00000426039.1:p.Ala21=
NM_000320.2:c.63T= NP_000311.2:p.Ala21=
NM_001306140.1:c.63T= NP_001293069.1:p.Ala21=
XR_241677.1:n.226T=
NR_156494.1:n.243T=
NM_000320.3:c.63T= MANE Select NP_000311.2:p.Ala21=
NM_001306140.2:c.63T= NP_001293069.1:p.Ala21=
NR_156494.2:n.99T=