Canonical Allele Identifier: CA1441595132
Gene: QDPR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.17511960G= , CM000666.2:g.17511960G= GRCh38
NC_000004.11:g.17513583G= , CM000666.1:g.17513583G= GRCh37
NC_000004.10:g.17122681G= NCBI36
NG_008763.1:g.5275C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000281243.10:c.95C= MANE Select ENSP00000281243.5:p.Ala32=
ENST00000281243.9:c.95C= ENSP00000281243.5:p.Ala32=
ENST00000428702.6:c.95C= ENSP00000390944.2:p.Ala32=
ENST00000505710.1:c.22C=
ENST00000507439.5:c.95C= ENSP00000423227.1:p.Ala32=
ENST00000508623.5:c.95C= ENSP00000426377.1:p.Ala32=
ENST00000513615.5:c.95C= ENSP00000422759.1:p.Ala32=
ENST00000514300.1:c.95C= ENSP00000426039.1:p.Ala32=
NM_000320.2:c.95C= NP_000311.2:p.Ala32=
NM_001306140.1:c.95C= NP_001293069.1:p.Ala32=
XR_241677.1:n.258C=
NR_156494.1:n.275C=
NM_000320.3:c.95C= MANE Select NP_000311.2:p.Ala32=
NM_001306140.2:c.95C= NP_001293069.1:p.Ala32=
NR_156494.2:n.131C=