Canonical Allele Identifier: CA438714121

Gene: QDPR

Linked Data

• MyVariant Identifiers: chr4:g.17506033T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.17504410T>A , CM000666.2:g.17504410T>A	GRCh38
NC_000004.11:g.17506033T>A , CM000666.1:g.17506033T>A	GRCh37
NC_000004.10:g.17115131T>A	NCBI36
NG_008763.1:g.12825A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000706645.1:n.1311A>T
ENST00000281243.10:c.264A>T MANE Select	ENSP00000281243.5:p.Gly88=
ENST00000281243.9:c.264A>T	ENSP00000281243.5:p.Gly88=
ENST00000428702.6:c.171A>T	ENSP00000390944.2:p.Gly57=
ENST00000505710.1:c.191A>T
ENST00000507439.5:c.264A>T	ENSP00000423227.1:p.Gly88=
ENST00000508623.5:c.264A>T	ENSP00000426377.1:p.Gly88=
ENST00000513615.5:c.264A>T	ENSP00000422759.1:p.Gly88=
ENST00000514300.1:c.*195A>T	ENSP00000426039.1:n.*195A>T
NM_000320.2:c.264A>T	NP_000311.2:p.Gly88=
NM_001306140.1:c.171A>T	NP_001293069.1:p.Gly57=
XR_241677.1:n.427A>T
NR_156494.1:n.444A>T
NM_000320.3:c.264A>T MANE Select	NP_000311.2:p.Gly88=
NM_001306140.2:c.171A>T	NP_001293069.1:p.Gly57=
NR_156494.2:n.300A>T