Canonical Allele Identifier: CA356454326

Gene: QDPR

Linked Data

• gnomAD v4: 4-17511973-G-C
• MyVariant Identifiers: chr4:g.17513596G>C (hg19) ; chr4:g.17511973G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.17511973G>C , CM000666.2:g.17511973G>C	GRCh38
NC_000004.11:g.17513596G>C , CM000666.1:g.17513596G>C	GRCh37
NC_000004.10:g.17122694G>C	NCBI36
NG_008763.1:g.5262C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281243.10:c.82C>G MANE Select	ENSP00000281243.5:p.Gln28Glu
ENST00000281243.9:c.82C>G	ENSP00000281243.5:p.Gln28Glu
ENST00000428702.6:c.82C>G	ENSP00000390944.2:p.Gln28Glu
ENST00000505710.1:c.9C>G
ENST00000507439.5:c.82C>G	ENSP00000423227.1:p.Gln28Glu
ENST00000508623.5:c.82C>G	ENSP00000426377.1:p.Gln28Glu
ENST00000513615.5:c.82C>G	ENSP00000422759.1:p.Gln28Glu
ENST00000514300.1:c.82C>G	ENSP00000426039.1:p.Gln28Glu
NM_000320.2:c.82C>G	NP_000311.2:p.Gln28Glu
NM_001306140.1:c.82C>G	NP_001293069.1:p.Gln28Glu
XR_241677.1:n.245C>G
NR_156494.1:n.262C>G
NM_000320.3:c.82C>G MANE Select	NP_000311.2:p.Gln28Glu
NM_001306140.2:c.82C>G	NP_001293069.1:p.Gln28Glu
NR_156494.2:n.118C>G