Canonical Allele Identifier: CA438714152

Gene: QDPR

Linked Data

• dbSNP Id: rs1577193057
• MyVariant Identifiers: chr4:g.17506039A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.17504416A>C , CM000666.2:g.17504416A>C	GRCh38
NC_000004.11:g.17506039A>C , CM000666.1:g.17506039A>C	GRCh37
NC_000004.10:g.17115137A>C	NCBI36
NG_008763.1:g.12819T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000706645.1:n.1305T>G
ENST00000281243.10:c.258T>G MANE Select	ENSP00000281243.5:p.Val86=
ENST00000281243.9:c.258T>G	ENSP00000281243.5:p.Val86=
ENST00000428702.6:c.165T>G	ENSP00000390944.2:p.Val55=
ENST00000505710.1:c.185T>G
ENST00000507439.5:c.258T>G	ENSP00000423227.1:p.Val86=
ENST00000508623.5:c.258T>G	ENSP00000426377.1:p.Val86=
ENST00000513615.5:c.258T>G	ENSP00000422759.1:p.Val86=
ENST00000514300.1:c.*189T>G	ENSP00000426039.1:n.*189T>G
NM_000320.2:c.258T>G	NP_000311.2:p.Val86=
NM_001306140.1:c.165T>G	NP_001293069.1:p.Val55=
XR_241677.1:n.421T>G
NR_156494.1:n.438T>G
NM_000320.3:c.258T>G MANE Select	NP_000311.2:p.Val86=
NM_001306140.2:c.165T>G	NP_001293069.1:p.Val55=
NR_156494.2:n.294T>G