Canonical Allele Identifier: CA1441586137
Gene: QDPR HGNC NCBI

Linked Data

dbSNP Id: rs758883698

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.17492358G>C , CM000666.2:g.17492358G>C GRCh38
NC_000004.11:g.17493981G>C , CM000666.1:g.17493981G>C GRCh37
NC_000004.10:g.17103079G>C NCBI36
NG_008763.1:g.24877C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000706645.1:n.1484-18C>G
ENST00000281243.10:c.437-18C>G MANE Select ENSP00000281243.5:n.437-18C>G
ENST00000281243.9:c.437-18C>G ENSP00000281243.5:n.437-18C>G
ENST00000428702.6:c.344-18C>G ENSP00000390944.2:n.344-18C>G
ENST00000501943.6:n.156C>G
ENST00000505710.1:c.364-1613C>G
ENST00000507439.5:c.437-1613C>G ENSP00000423227.1:n.437-1613C>G
ENST00000508623.5:c.437-5122C>G ENSP00000426377.1:n.437-5122C>G
ENST00000511609.1:n.151C>G
ENST00000513615.5:c.437-1613C>G ENSP00000422759.1:n.437-1613C>G
ENST00000514300.1:c.*368-1613C>G ENSP00000426039.1:n.*368-1613C>G
NM_000320.2:c.437-18C>G NP_000311.2:n.437-18C>G
NM_001306140.1:c.344-18C>G NP_001293069.1:n.344-18C>G
XR_241677.1:n.600-1613C>G
NR_156494.1:n.617-1613C>G
NM_000320.3:c.437-18C>G MANE Select NP_000311.2:n.437-18C>G
NM_001306140.2:c.344-18C>G NP_001293069.1:n.344-18C>G
NR_156494.2:n.473-1613C>G