Canonical Allele Identifier: CA2578051112

Gene: QDPR

Linked Data

• gnomAD v4: 4-17492440-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.17492440A>T , CM000666.2:g.17492440A>T	GRCh38
NC_000004.11:g.17494063A>T , CM000666.1:g.17494063A>T	GRCh37
NC_000004.10:g.17103161A>T	NCBI36
NG_008763.1:g.24795T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706645.1:n.1484-100T>A
ENST00000281243.10:c.437-100T>A MANE Select	ENSP00000281243.5:n.437-100T>A
ENST00000281243.9:c.437-100T>A	ENSP00000281243.5:n.437-100T>A
ENST00000428702.6:c.344-100T>A	ENSP00000390944.2:n.344-100T>A
ENST00000501943.6:n.74T>A
ENST00000505710.1:c.364-1695T>A
ENST00000507439.5:c.437-1695T>A	ENSP00000423227.1:n.437-1695T>A
ENST00000508623.5:c.437-5204T>A	ENSP00000426377.1:n.437-5204T>A
ENST00000511609.1:n.69T>A
ENST00000513615.5:c.437-1695T>A	ENSP00000422759.1:n.437-1695T>A
ENST00000514300.1:c.*368-1695T>A	ENSP00000426039.1:n.*368-1695T>A
NM_000320.2:c.437-100T>A	NP_000311.2:n.437-100T>A
NM_001306140.1:c.344-100T>A	NP_001293069.1:n.344-100T>A
XR_241677.1:n.600-1695T>A
NR_156494.1:n.617-1695T>A
NM_000320.3:c.437-100T>A MANE Select	NP_000311.2:n.437-100T>A
NM_001306140.2:c.344-100T>A	NP_001293069.1:n.344-100T>A
NR_156494.2:n.473-1695T>A