Canonical Allele Identifier: CA356454322
Gene: QDPR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.17511972T>A , CM000666.2:g.17511972T>A GRCh38
NC_000004.11:g.17513595T>A , CM000666.1:g.17513595T>A GRCh37
NC_000004.10:g.17122693T>A NCBI36
NG_008763.1:g.5263A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000281243.10:c.83A>T MANE Select ENSP00000281243.5:p.Gln28Leu
ENST00000281243.9:c.83A>T ENSP00000281243.5:p.Gln28Leu
ENST00000428702.6:c.83A>T ENSP00000390944.2:p.Gln28Leu
ENST00000505710.1:c.10A>T
ENST00000507439.5:c.83A>T ENSP00000423227.1:p.Gln28Leu
ENST00000508623.5:c.83A>T ENSP00000426377.1:p.Gln28Leu
ENST00000513615.5:c.83A>T ENSP00000422759.1:p.Gln28Leu
ENST00000514300.1:c.83A>T ENSP00000426039.1:p.Gln28Leu
NM_000320.2:c.83A>T NP_000311.2:p.Gln28Leu
NM_001306140.1:c.83A>T NP_001293069.1:p.Gln28Leu
XR_241677.1:n.246A>T
NR_156494.1:n.263A>T
NM_000320.3:c.83A>T MANE Select NP_000311.2:p.Gln28Leu
NM_001306140.2:c.83A>T NP_001293069.1:p.Gln28Leu
NR_156494.2:n.119A>T