Canonical Allele Identifier: CA1441585861

Gene: QDPR

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.17491793_17491794delinsAC , CM000666.2:g.17491793_17491794delinsAC	GRCh38
NC_000004.11:g.17493416_17493417delinsAC , CM000666.1:g.17493416_17493417delinsAC	GRCh37
NC_000004.10:g.17102514_17102515delinsAC	NCBI36
NG_008763.1:g.25441_25442delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706645.1:n.1592+438_1592+439delinsGT
ENST00000281243.10:c.545+438_545+439delinsGT MANE Select	ENSP00000281243.5:n.545+438_545+439delinsGT
ENST00000281243.9:c.545+438_545+439delinsGT	ENSP00000281243.5:n.545+438_545+439delinsGT
ENST00000428702.6:c.452+438_452+439delinsGT	ENSP00000390944.2:n.452+438_452+439delinsGT
ENST00000501943.6:n.282+438_282+439delinsGT
ENST00000505710.1:c.364-1049_364-1048delinsGT
ENST00000507439.5:c.437-1049_437-1048delinsGT	ENSP00000423227.1:n.437-1049_437-1048delinsGT
ENST00000508623.5:c.437-4558_437-4557delinsGT	ENSP00000426377.1:n.437-4558_437-4557delinsGT
ENST00000511609.1:n.277+438_277+439delinsGT
ENST00000513615.5:c.437-1049_437-1048delinsGT	ENSP00000422759.1:n.437-1049_437-1048delinsGT
ENST00000514300.1:c.*368-1049_*368-1048delinsGT	ENSP00000426039.1:n.*368-1049_*368-1048delinsGT
NM_000320.2:c.545+438_545+439delinsGT	NP_000311.2:n.545+438_545+439delinsGT
NM_001306140.1:c.452+438_452+439delinsGT	NP_001293069.1:n.452+438_452+439delinsGT
XR_241677.1:n.600-1049_600-1048delinsGT
NR_156494.1:n.617-1049_617-1048delinsGT
NM_000320.3:c.545+438_545+439delinsGT MANE Select	NP_000311.2:n.545+438_545+439delinsGT
NM_001306140.2:c.452+438_452+439delinsGT	NP_001293069.1:n.452+438_452+439delinsGT
NR_156494.2:n.473-1049_473-1048delinsGT