Canonical Allele Identifier: CA2340885466
Gene: POLD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50406949C= , CM000681.2:g.50406949C= GRCh38
NC_000019.9:g.50910206C= , CM000681.1:g.50910206C= GRCh37
NC_000019.8:g.55602018C= NCBI36
NG_033800.1:g.27627C= , LRG_785:g.27627C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000593887.2:c.1495-34C= ENSP00000472607.2:n.1495-34C=
ENST00000600746.2:n.1686-34C=
ENST00000644560.2:c.1495-34C= ENSP00000495618.2:n.1495-34C=
ENST00000687454.1:c.1495-34C= ENSP00000510052.1:n.1495-34C=
ENST00000440232.7:c.1495-34C= MANE Select ENSP00000406046.1:n.1495-34C=
ENST00000595904.6:c.1495-34C= ENSP00000472445.1:n.1495-34C=
ENST00000599857.7:c.1495-34C= ENSP00000473052.1:n.1495-34C=
ENST00000601098.6:c.1495-34C= ENSP00000472600.2:n.1495-34C=
ENST00000613923.6:c.1495-34C= ENSP00000481858.2:n.1495-34C=
ENST00000643407.1:c.1495-34C= ENSP00000496078.1:n.1495-34C=
ENST00000644560.1:c.366-34C=
ENST00000440232.6:c.1495-34C= ENSP00000406046.1:n.1495-34C=
ENST00000595904.5:c.1495-34C= ENSP00000472445.1:n.1495-34C=
ENST00000599857.5:c.1495-34C= ENSP00000473052.1:n.1495-34C=
ENST00000600859.5:c.1495-34C= ENSP00000470726.1:n.1495-34C=
ENST00000613923.4:c.1495-34C= ENSP00000481858.1:n.1495-34C=
NM_001256849.1:c.1495-34C= , LRG_785t1:c.1495-34C= NP_001243778.1:n.1495-34C=
NM_001308632.1:c.1495-34C= , LRG_785t2:c.1495-34C= NP_001295561.1:n.1495-34C=
NM_002691.3:c.1495-34C= NP_002682.2:n.1495-34C=
NR_046402.1:n.1564-34C=
XM_005259008.3:c.1495-34C= XP_005259065.1:n.1495-34C=
XM_011527038.1:c.1495-34C= XP_011525340.1:n.1495-34C=
XM_011527039.1:c.1495-34C= XP_011525341.1:n.1495-34C=
XR_935835.1:n.1597-34C=
XM_005259008.4:c.1495-34C= XP_005259065.1:n.1495-34C=
XM_017026881.1:c.1495-34C= XP_016882370.1:n.1495-34C=
XM_017026882.2:c.1495-34C= XP_016882371.1:n.1495-34C=
XR_935835.2:n.1596-34C=
NM_002691.4:c.1495-34C= MANE Select NP_002682.2:n.1495-34C=
NR_046402.2:n.1540-34C=