Canonical Allele Identifier: CA1441586085

Gene: QDPR

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.17492249G= , CM000666.2:g.17492249G=	GRCh38
NC_000004.11:g.17493872G= , CM000666.1:g.17493872G=	GRCh37
NC_000004.10:g.17102970G=	NCBI36
NG_008763.1:g.24986C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706645.1:n.1575C=
ENST00000281243.10:c.528C= MANE Select	ENSP00000281243.5:p.Ala176=
ENST00000281243.9:c.528C=	ENSP00000281243.5:p.Ala176=
ENST00000428702.6:c.435C=	ENSP00000390944.2:p.Ala145=
ENST00000501943.6:n.265C=
ENST00000505710.1:c.364-1504C=
ENST00000507439.5:c.437-1504C=	ENSP00000423227.1:n.437-1504C=
ENST00000508623.5:c.437-5013C=	ENSP00000426377.1:n.437-5013C=
ENST00000511609.1:n.260C=
ENST00000513615.5:c.437-1504C=	ENSP00000422759.1:n.437-1504C=
ENST00000514300.1:c.*368-1504C=	ENSP00000426039.1:n.*368-1504C=
NM_000320.2:c.528C=	NP_000311.2:p.Ala176=
NM_001306140.1:c.435C=	NP_001293069.1:p.Ala145=
XR_241677.1:n.600-1504C=
NR_156494.1:n.617-1504C=
NM_000320.3:c.528C= MANE Select	NP_000311.2:p.Ala176=
NM_001306140.2:c.435C=	NP_001293069.1:p.Ala145=
NR_156494.2:n.473-1504C=