Canonical Allele Identifier: CA1441586099

Gene: QDPR

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.17492272T= , CM000666.2:g.17492272T=	GRCh38
NC_000004.11:g.17493895T= , CM000666.1:g.17493895T=	GRCh37
NC_000004.10:g.17102993T=	NCBI36
NG_008763.1:g.24963A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706645.1:n.1552A=
ENST00000281243.10:c.505A= MANE Select	ENSP00000281243.5:p.Ser169=
ENST00000281243.9:c.505A=	ENSP00000281243.5:p.Ser169=
ENST00000428702.6:c.412A=	ENSP00000390944.2:p.Ser138=
ENST00000501943.6:n.242A=
ENST00000505710.1:c.364-1527A=
ENST00000507439.5:c.437-1527A=	ENSP00000423227.1:n.437-1527A=
ENST00000508623.5:c.437-5036A=	ENSP00000426377.1:n.437-5036A=
ENST00000511609.1:n.237A=
ENST00000513615.5:c.437-1527A=	ENSP00000422759.1:n.437-1527A=
ENST00000514300.1:c.*368-1527A=	ENSP00000426039.1:n.*368-1527A=
NM_000320.2:c.505A=	NP_000311.2:p.Ser169=
NM_001306140.1:c.412A=	NP_001293069.1:p.Ser138=
XR_241677.1:n.600-1527A=
NR_156494.1:n.617-1527A=
NM_000320.3:c.505A= MANE Select	NP_000311.2:p.Ser169=
NM_001306140.2:c.412A=	NP_001293069.1:p.Ser138=
NR_156494.2:n.473-1527A=