Canonical Allele Identifier: CA1441595152
Gene: QDPR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.17511999C= , CM000666.2:g.17511999C= GRCh38
NC_000004.11:g.17513622C= , CM000666.1:g.17513622C= GRCh37
NC_000004.10:g.17122720C= NCBI36
NG_008763.1:g.5236G=

Transcript Alleles

HGVS Amino-acid change
ENST00000281243.10:c.56G= MANE Select ENSP00000281243.5:p.Arg19=
ENST00000281243.9:c.56G= ENSP00000281243.5:p.Arg19=
ENST00000428702.6:c.56G= ENSP00000390944.2:p.Arg19=
ENST00000507439.5:c.56G= ENSP00000423227.1:p.Arg19=
ENST00000508623.5:c.56G= ENSP00000426377.1:p.Arg19=
ENST00000513615.5:c.56G= ENSP00000422759.1:p.Arg19=
ENST00000514300.1:c.56G= ENSP00000426039.1:p.Arg19=
NM_000320.2:c.56G= NP_000311.2:p.Arg19=
NM_001306140.1:c.56G= NP_001293069.1:p.Arg19=
XR_241677.1:n.219G=
NR_156494.1:n.236G=
NM_000320.3:c.56G= MANE Select NP_000311.2:p.Arg19=
NM_001306140.2:c.56G= NP_001293069.1:p.Arg19=
NR_156494.2:n.92G=