Canonical Allele Identifier: CA1441590377
Community Standard Title: NM_000320.3(QDPR):c.322T= (p.Trp108=)
Gene: QDPR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.17501833A= , CM000666.2:g.17501833A= GRCh38
NC_000004.11:g.17503456A= , CM000666.1:g.17503456A= GRCh37
NC_000004.10:g.17112554A= NCBI36
NG_008763.1:g.15402T=

Transcript Alleles

HGVS Amino-acid Change
NM_000320.3:c.322T= MANE Select NP_000311.2:p.Trp108=
ENST00000281243.10:c.322T= MANE Select ENSP00000281243.5:p.Trp108=
NM_000320.2:c.322T= NP_000311.2:p.Trp108=
NM_001306140.1:c.229T= NP_001293069.1:p.Trp77=
NM_001306140.2:c.229T= NP_001293069.1:p.Trp77=
NR_156494.1:n.502T=
NR_156494.2:n.358T=
ENST00000281243.9:c.322T= ENSP00000281243.5:p.Trp108=
ENST00000428702.6:c.229T= ENSP00000390944.2:p.Trp77=
ENST00000505710.1:c.249T=
ENST00000507439.5:c.322T= ENSP00000423227.1:p.Trp108=
ENST00000508623.5:c.322T= ENSP00000426377.1:p.Trp108=
ENST00000513615.5:c.322T= ENSP00000422759.1:p.Trp108=
ENST00000514300.1:c.*253T= ENSP00000426039.1:n.*253T=
ENST00000706645.1:n.1369T=
XR_241677.1:n.485T=