Canonical Allele Identifier: CA348105
Gene: POLD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 220847
dbSNP Id: rs149096523

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50402329G>A , CM000681.2:g.50402329G>A GRCh38
NC_000019.9:g.50905586G>A , CM000681.1:g.50905586G>A GRCh37
NC_000019.8:g.55597398G>A NCBI36
NG_033800.1:g.23007G>A , LRG_785:g.23007G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000593887.2:c.714G>A ENSP00000472607.2:p.Thr238=
ENST00000600746.2:n.905G>A
ENST00000644560.2:c.714G>A ENSP00000495618.2:p.Thr238=
ENST00000687454.1:c.714G>A ENSP00000510052.1:p.Thr238=
ENST00000440232.7:c.714G>A MANE Select ENSP00000406046.1:p.Thr238=
ENST00000595904.6:c.714G>A ENSP00000472445.1:p.Thr238=
ENST00000599857.7:c.714G>A ENSP00000473052.1:p.Thr238=
ENST00000601098.6:c.714G>A ENSP00000472600.2:p.Thr238=
ENST00000613923.6:c.714G>A ENSP00000481858.2:p.Thr238=
ENST00000643407.1:c.714G>A ENSP00000496078.1:p.Thr238=
ENST00000440232.6:c.714G>A ENSP00000406046.1:p.Thr238=
ENST00000595904.5:c.714G>A ENSP00000472445.1:p.Thr238=
ENST00000599857.5:c.714G>A ENSP00000473052.1:p.Thr238=
ENST00000600746.1:n.819G>A
ENST00000600859.5:c.714G>A ENSP00000470726.1:p.Thr238=
ENST00000613923.4:c.714G>A ENSP00000481858.1:p.Thr238=
NM_001256849.1:c.714G>A , LRG_785t1:c.714G>A NP_001243778.1:p.Thr238=
NM_001308632.1:c.714G>A , LRG_785t2:c.714G>A NP_001295561.1:p.Thr238=
NM_002691.3:c.714G>A NP_002682.2:p.Thr238=
NR_046402.1:n.783G>A
XM_005259008.3:c.714G>A XP_005259065.1:p.Thr238=
XM_011527038.1:c.714G>A XP_011525340.1:p.Thr238=
XM_011527039.1:c.714G>A XP_011525341.1:p.Thr238=
XR_935835.1:n.816G>A
XM_005259008.4:c.714G>A XP_005259065.1:p.Thr238=
XM_017026881.1:c.714G>A XP_016882370.1:p.Thr238=
XM_017026882.2:c.714G>A XP_016882371.1:p.Thr238=
XR_935835.2:n.815G>A
NM_002691.4:c.714G>A MANE Select NP_002682.2:p.Thr238=
NR_046402.2:n.759G>A