Canonical Allele Identifier: CA438716073

Gene: QDPR

Linked Data

• MyVariant Identifiers: chr4:g.17513624G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.17512001G>A , CM000666.2:g.17512001G>A	GRCh38
NC_000004.11:g.17513624G>A , CM000666.1:g.17513624G>A	GRCh37
NC_000004.10:g.17122722G>A	NCBI36
NG_008763.1:g.5234C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281243.10:c.54C>T MANE Select	ENSP00000281243.5:p.Gly18=
ENST00000281243.9:c.54C>T	ENSP00000281243.5:p.Gly18=
ENST00000428702.6:c.54C>T	ENSP00000390944.2:p.Gly18=
ENST00000507439.5:c.54C>T	ENSP00000423227.1:p.Gly18=
ENST00000508623.5:c.54C>T	ENSP00000426377.1:p.Gly18=
ENST00000513615.5:c.54C>T	ENSP00000422759.1:p.Gly18=
ENST00000514300.1:c.54C>T	ENSP00000426039.1:p.Gly18=
NM_000320.2:c.54C>T	NP_000311.2:p.Gly18=
NM_001306140.1:c.54C>T	NP_001293069.1:p.Gly18=
XR_241677.1:n.217C>T
NR_156494.1:n.234C>T
NM_000320.3:c.54C>T MANE Select	NP_000311.2:p.Gly18=
NM_001306140.2:c.54C>T	NP_001293069.1:p.Gly18=
NR_156494.2:n.90C>T