Canonical Allele Identifier: CA438712379

Gene: QDPR

Linked Data

• dbSNP Id: rs766608406
• gnomAD v2: 4-17493947-G-A
• MyVariant Identifiers: chr4:g.17493947G>A (hg19) ; chr4:g.17492324G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.17492324G>A , CM000666.2:g.17492324G>A	GRCh38
NC_000004.11:g.17493947G>A , CM000666.1:g.17493947G>A	GRCh37
NC_000004.10:g.17103045G>A	NCBI36
NG_008763.1:g.24911C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706645.1:n.1500C>T
ENST00000281243.10:c.453C>T MANE Select	ENSP00000281243.5:p.Gly151=
ENST00000281243.9:c.453C>T	ENSP00000281243.5:p.Gly151=
ENST00000428702.6:c.360C>T	ENSP00000390944.2:p.Gly120=
ENST00000501943.6:n.190C>T
ENST00000505710.1:c.364-1579C>T
ENST00000507439.5:c.437-1579C>T	ENSP00000423227.1:n.437-1579C>T
ENST00000508623.5:c.437-5088C>T	ENSP00000426377.1:n.437-5088C>T
ENST00000511609.1:n.185C>T
ENST00000513615.5:c.437-1579C>T	ENSP00000422759.1:n.437-1579C>T
ENST00000514300.1:c.*368-1579C>T	ENSP00000426039.1:n.*368-1579C>T
NM_000320.2:c.453C>T	NP_000311.2:p.Gly151=
NM_001306140.1:c.360C>T	NP_001293069.1:p.Gly120=
XR_241677.1:n.600-1579C>T
NR_156494.1:n.617-1579C>T
NM_000320.3:c.453C>T MANE Select	NP_000311.2:p.Gly151=
NM_001306140.2:c.360C>T	NP_001293069.1:p.Gly120=
NR_156494.2:n.473-1579C>T