Canonical Allele Identifier: CA356444895

Gene: QDPR

Linked Data

• MyVariant Identifiers: chr4:g.17493959C>G (hg19) ; chr4:g.17492336C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.17492336C>G , CM000666.2:g.17492336C>G	GRCh38
NC_000004.11:g.17493959C>G , CM000666.1:g.17493959C>G	GRCh37
NC_000004.10:g.17103057C>G	NCBI36
NG_008763.1:g.24899G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000706645.1:n.1488G>C
ENST00000281243.10:c.441G>C MANE Select	ENSP00000281243.5:p.Met147Ile
ENST00000281243.9:c.441G>C	ENSP00000281243.5:p.Met147Ile
ENST00000428702.6:c.348G>C	ENSP00000390944.2:p.Met116Ile
ENST00000501943.6:n.178G>C
ENST00000505710.1:c.364-1591G>C
ENST00000507439.5:c.437-1591G>C	ENSP00000423227.1:n.437-1591G>C
ENST00000508623.5:c.437-5100G>C	ENSP00000426377.1:n.437-5100G>C
ENST00000511609.1:n.173G>C
ENST00000513615.5:c.437-1591G>C	ENSP00000422759.1:n.437-1591G>C
ENST00000514300.1:c.*368-1591G>C	ENSP00000426039.1:n.*368-1591G>C
NM_000320.2:c.441G>C	NP_000311.2:p.Met147Ile
NM_001306140.1:c.348G>C	NP_001293069.1:p.Met116Ile
XR_241677.1:n.600-1591G>C
NR_156494.1:n.617-1591G>C
NM_000320.3:c.441G>C MANE Select	NP_000311.2:p.Met147Ile
NM_001306140.2:c.348G>C	NP_001293069.1:p.Met116Ile
NR_156494.2:n.473-1591G>C