Canonical Allele Identifier: CA2670124409

Gene: QDPR

Linked Data

• gnomAD v4: 4-17492452-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.17492452A>C , CM000666.2:g.17492452A>C	GRCh38
NC_000004.11:g.17494075A>C , CM000666.1:g.17494075A>C	GRCh37
NC_000004.10:g.17103173A>C	NCBI36
NG_008763.1:g.24783T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706645.1:n.1484-112T>G
ENST00000281243.10:c.437-112T>G MANE Select	ENSP00000281243.5:n.437-112T>G
ENST00000281243.9:c.437-112T>G	ENSP00000281243.5:n.437-112T>G
ENST00000428702.6:c.344-112T>G	ENSP00000390944.2:n.344-112T>G
ENST00000501943.6:n.62T>G
ENST00000505710.1:c.364-1707T>G
ENST00000507439.5:c.437-1707T>G	ENSP00000423227.1:n.437-1707T>G
ENST00000508623.5:c.437-5216T>G	ENSP00000426377.1:n.437-5216T>G
ENST00000511609.1:n.57T>G
ENST00000513615.5:c.437-1707T>G	ENSP00000422759.1:n.437-1707T>G
ENST00000514300.1:c.*368-1707T>G	ENSP00000426039.1:n.*368-1707T>G
NM_000320.2:c.437-112T>G	NP_000311.2:n.437-112T>G
NM_001306140.1:c.344-112T>G	NP_001293069.1:n.344-112T>G
XR_241677.1:n.600-1707T>G
NR_156494.1:n.617-1707T>G
NM_000320.3:c.437-112T>G MANE Select	NP_000311.2:n.437-112T>G
NM_001306140.2:c.344-112T>G	NP_001293069.1:n.344-112T>G
NR_156494.2:n.473-1707T>G