Canonical Allele Identifier: CA356453672
Gene: QDPR HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.17510986A>T (hg19) chr4:g.17509363A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.17509363A>T , CM000666.2:g.17509363A>T GRCh38
NC_000004.11:g.17510986A>T , CM000666.1:g.17510986A>T GRCh37
NC_000004.10:g.17120084A>T NCBI36
NG_008763.1:g.7872T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000706645.1:n.1153T>A
ENST00000281243.10:c.106T>A MANE Select ENSP00000281243.5:p.Trp36Arg
ENST00000281243.9:c.106T>A ENSP00000281243.5:p.Trp36Arg
ENST00000428702.6:c.105+2587T>A ENSP00000390944.2:n.105+2587T>A
ENST00000505710.1:c.33T>A
ENST00000507439.5:c.106T>A ENSP00000423227.1:p.Trp36Arg
ENST00000508623.5:c.106T>A ENSP00000426377.1:p.Trp36Arg
ENST00000513615.5:c.106T>A ENSP00000422759.1:p.Trp36Arg
ENST00000514300.1:c.*37T>A ENSP00000426039.1:n.*37T>A
NM_000320.2:c.106T>A NP_000311.2:p.Trp36Arg
NM_001306140.1:c.105+2587T>A NP_001293069.1:n.105+2587T>A
XR_241677.1:n.269T>A
NR_156494.1:n.286T>A
NM_000320.3:c.106T>A MANE Select NP_000311.2:p.Trp36Arg
NM_001306140.2:c.105+2587T>A NP_001293069.1:n.105+2587T>A
NR_156494.2:n.142T>A
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