Canonical Allele Identifier: CA2670122136

Gene: QDPR

Linked Data

• gnomAD v4: 4-17504328-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.17504328G>T , CM000666.2:g.17504328G>T	GRCh38
NC_000004.11:g.17505951G>T , CM000666.1:g.17505951G>T	GRCh37
NC_000004.10:g.17115049G>T	NCBI36
NG_008763.1:g.12907C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000706645.1:n.1342+51C>A
ENST00000281243.10:c.295+51C>A MANE Select	ENSP00000281243.5:n.295+51C>A
ENST00000281243.9:c.295+51C>A	ENSP00000281243.5:n.295+51C>A
ENST00000428702.6:c.202+51C>A	ENSP00000390944.2:n.202+51C>A
ENST00000505710.1:c.222+51C>A
ENST00000507439.5:c.295+51C>A	ENSP00000423227.1:n.295+51C>A
ENST00000508623.5:c.295+51C>A	ENSP00000426377.1:n.295+51C>A
ENST00000513615.5:c.295+51C>A	ENSP00000422759.1:n.295+51C>A
ENST00000514300.1:c.*226+51C>A	ENSP00000426039.1:n.*226+51C>A
NM_000320.2:c.295+51C>A	NP_000311.2:n.295+51C>A
NM_001306140.1:c.202+51C>A	NP_001293069.1:n.202+51C>A
XR_241677.1:n.458+51C>A
NR_156494.1:n.475+51C>A
NM_000320.3:c.295+51C>A MANE Select	NP_000311.2:n.295+51C>A
NM_001306140.2:c.202+51C>A	NP_001293069.1:n.202+51C>A
NR_156494.2:n.331+51C>A