Canonical Allele Identifier: CA1441595122
Gene: QDPR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.17511946T= , CM000666.2:g.17511946T= GRCh38
NC_000004.11:g.17513569T= , CM000666.1:g.17513569T= GRCh37
NC_000004.10:g.17122667T= NCBI36
NG_008763.1:g.5289A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000281243.10:c.105+4A= MANE Select ENSP00000281243.5:n.105+4A=
ENST00000281243.9:c.105+4A= ENSP00000281243.5:n.105+4A=
ENST00000428702.6:c.105+4A= ENSP00000390944.2:n.105+4A=
ENST00000505710.1:c.32+4A=
ENST00000507439.5:c.105+4A= ENSP00000423227.1:n.105+4A=
ENST00000508623.5:c.105+4A= ENSP00000426377.1:n.105+4A=
ENST00000513615.5:c.105+4A= ENSP00000422759.1:n.105+4A=
ENST00000514300.1:c.105+4A= ENSP00000426039.1:n.105+4A=
NM_000320.2:c.105+4A= NP_000311.2:n.105+4A=
NM_001306140.1:c.105+4A= NP_001293069.1:n.105+4A=
XR_241677.1:n.268+4A=
NR_156494.1:n.285+4A=
NM_000320.3:c.105+4A= MANE Select NP_000311.2:n.105+4A=
NM_001306140.2:c.105+4A= NP_001293069.1:n.105+4A=
NR_156494.2:n.141+4A=