Canonical Allele Identifier: CA438714112

Gene: QDPR

Linked Data

• MyVariant Identifiers: chr4:g.17506030T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.17504407T>G , CM000666.2:g.17504407T>G	GRCh38
NC_000004.11:g.17506030T>G , CM000666.1:g.17506030T>G	GRCh37
NC_000004.10:g.17115128T>G	NCBI36
NG_008763.1:g.12828A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000706645.1:n.1314A>C
ENST00000281243.10:c.267A>C MANE Select	ENSP00000281243.5:p.Gly89=
ENST00000281243.9:c.267A>C	ENSP00000281243.5:p.Gly89=
ENST00000428702.6:c.174A>C	ENSP00000390944.2:p.Gly58=
ENST00000505710.1:c.194A>C
ENST00000507439.5:c.267A>C	ENSP00000423227.1:p.Gly89=
ENST00000508623.5:c.267A>C	ENSP00000426377.1:p.Gly89=
ENST00000513615.5:c.267A>C	ENSP00000422759.1:p.Gly89=
ENST00000514300.1:c.*198A>C	ENSP00000426039.1:n.*198A>C
NM_000320.2:c.267A>C	NP_000311.2:p.Gly89=
NM_001306140.1:c.174A>C	NP_001293069.1:p.Gly58=
XR_241677.1:n.430A>C
NR_156494.1:n.447A>C
NM_000320.3:c.267A>C MANE Select	NP_000311.2:p.Gly89=
NM_001306140.2:c.174A>C	NP_001293069.1:p.Gly58=
NR_156494.2:n.303A>C