Canonical Allele Identifier: CA1441585901

Gene: QDPR

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.17491863A= , CM000666.2:g.17491863A=	GRCh38
NC_000004.11:g.17493486A= , CM000666.1:g.17493486A=	GRCh37
NC_000004.10:g.17102584A=	NCBI36
NG_008763.1:g.25372T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706645.1:n.1592+369T=
ENST00000281243.10:c.545+369T= MANE Select	ENSP00000281243.5:n.545+369T=
ENST00000281243.9:c.545+369T=	ENSP00000281243.5:n.545+369T=
ENST00000428702.6:c.452+369T=	ENSP00000390944.2:n.452+369T=
ENST00000501943.6:n.282+369T=
ENST00000505710.1:c.364-1118T=
ENST00000507439.5:c.437-1118T=	ENSP00000423227.1:n.437-1118T=
ENST00000508623.5:c.437-4627T=	ENSP00000426377.1:n.437-4627T=
ENST00000511609.1:n.277+369T=
ENST00000513615.5:c.437-1118T=	ENSP00000422759.1:n.437-1118T=
ENST00000514300.1:c.*368-1118T=	ENSP00000426039.1:n.*368-1118T=
NM_000320.2:c.545+369T=	NP_000311.2:n.545+369T=
NM_001306140.1:c.452+369T=	NP_001293069.1:n.452+369T=
XR_241677.1:n.600-1118T=
NR_156494.1:n.617-1118T=
NM_000320.3:c.545+369T= MANE Select	NP_000311.2:n.545+369T=
NM_001306140.2:c.452+369T=	NP_001293069.1:n.452+369T=
NR_156494.2:n.473-1118T=