Canonical Allele Identifier: CA438712346

Gene: QDPR

Linked Data

• MyVariant Identifiers: chr4:g.17493935A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.17492312A>C , CM000666.2:g.17492312A>C	GRCh38
NC_000004.11:g.17493935A>C , CM000666.1:g.17493935A>C	GRCh37
NC_000004.10:g.17103033A>C	NCBI36
NG_008763.1:g.24923T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706645.1:n.1512T>G
ENST00000281243.10:c.465T>G MANE Select	ENSP00000281243.5:p.Gly155=
ENST00000281243.9:c.465T>G	ENSP00000281243.5:p.Gly155=
ENST00000428702.6:c.372T>G	ENSP00000390944.2:p.Gly124=
ENST00000501943.6:n.202T>G
ENST00000505710.1:c.364-1567T>G
ENST00000507439.5:c.437-1567T>G	ENSP00000423227.1:n.437-1567T>G
ENST00000508623.5:c.437-5076T>G	ENSP00000426377.1:n.437-5076T>G
ENST00000511609.1:n.197T>G
ENST00000513615.5:c.437-1567T>G	ENSP00000422759.1:n.437-1567T>G
ENST00000514300.1:c.*368-1567T>G	ENSP00000426039.1:n.*368-1567T>G
NM_000320.2:c.465T>G	NP_000311.2:p.Gly155=
NM_001306140.1:c.372T>G	NP_001293069.1:p.Gly124=
XR_241677.1:n.600-1567T>G
NR_156494.1:n.617-1567T>G
NM_000320.3:c.465T>G MANE Select	NP_000311.2:p.Gly155=
NM_001306140.2:c.372T>G	NP_001293069.1:p.Gly124=
NR_156494.2:n.473-1567T>G