Canonical Allele Identifier: CA791226411

Gene: QDPR

Linked Data

• dbSNP Id: rs1272088125
• gnomAD v4: 4-17492131-G-C
• MyVariant Identifiers: chr4:g.17493754G>C (hg19) ; chr4:g.17492131G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.17492131G>C , CM000666.2:g.17492131G>C	GRCh38
NC_000004.11:g.17493754G>C , CM000666.1:g.17493754G>C	GRCh37
NC_000004.10:g.17102852G>C	NCBI36
NG_008763.1:g.25104C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706645.1:n.1592+101C>G
ENST00000281243.10:c.545+101C>G MANE Select	ENSP00000281243.5:n.545+101C>G
ENST00000281243.9:c.545+101C>G	ENSP00000281243.5:n.545+101C>G
ENST00000428702.6:c.452+101C>G	ENSP00000390944.2:n.452+101C>G
ENST00000501943.6:n.282+101C>G
ENST00000505710.1:c.364-1386C>G
ENST00000507439.5:c.437-1386C>G	ENSP00000423227.1:n.437-1386C>G
ENST00000508623.5:c.437-4895C>G	ENSP00000426377.1:n.437-4895C>G
ENST00000511609.1:n.277+101C>G
ENST00000513615.5:c.437-1386C>G	ENSP00000422759.1:n.437-1386C>G
ENST00000514300.1:c.*368-1386C>G	ENSP00000426039.1:n.*368-1386C>G
NM_000320.2:c.545+101C>G	NP_000311.2:n.545+101C>G
NM_001306140.1:c.452+101C>G	NP_001293069.1:n.452+101C>G
XR_241677.1:n.600-1386C>G
NR_156494.1:n.617-1386C>G
NM_000320.3:c.545+101C>G MANE Select	NP_000311.2:n.545+101C>G
NM_001306140.2:c.452+101C>G	NP_001293069.1:n.452+101C>G
NR_156494.2:n.473-1386C>G