Canonical Allele Identifier: CA2340882666

Gene: POLD1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50402181_50402183delinsGGT , CM000681.2:g.50402181_50402183delinsGGT	GRCh38
NC_000019.9:g.50905438_50905440delinsGGT , CM000681.1:g.50905438_50905440delinsGGT	GRCh37
NC_000019.8:g.55597250_55597252delinsGGT	NCBI36
NG_033800.1:g.22859_22861delinsGGT , LRG_785:g.22859_22861delinsGGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593887.2:c.590-24_590-22delinsGGT	ENSP00000472607.2:n.590-24_590-22delinsGGT
ENST00000600746.2:n.757_759delinsGGT
ENST00000644560.2:c.590-24_590-22delinsGGT	ENSP00000495618.2:n.590-24_590-22delinsGGT
ENST00000687454.1:c.590-24_590-22delinsGGT	ENSP00000510052.1:n.590-24_590-22delinsGGT
ENST00000440232.7:c.590-24_590-22delinsGGT MANE Select	ENSP00000406046.1:n.590-24_590-22delinsGGT
ENST00000595904.6:c.590-24_590-22delinsGGT	ENSP00000472445.1:n.590-24_590-22delinsGGT
ENST00000599857.7:c.590-24_590-22delinsGGT	ENSP00000473052.1:n.590-24_590-22delinsGGT
ENST00000601098.6:c.590-24_590-22delinsGGT	ENSP00000472600.2:n.590-24_590-22delinsGGT
ENST00000613923.6:c.590-24_590-22delinsGGT	ENSP00000481858.2:n.590-24_590-22delinsGGT
ENST00000643407.1:c.590-24_590-22delinsGGT	ENSP00000496078.1:n.590-24_590-22delinsGGT
ENST00000440232.6:c.590-24_590-22delinsGGT	ENSP00000406046.1:n.590-24_590-22delinsGGT
ENST00000595904.5:c.590-24_590-22delinsGGT	ENSP00000472445.1:n.590-24_590-22delinsGGT
ENST00000599857.5:c.590-24_590-22delinsGGT	ENSP00000473052.1:n.590-24_590-22delinsGGT
ENST00000600746.1:n.671_673delinsGGT
ENST00000600859.5:c.590-24_590-22delinsGGT	ENSP00000470726.1:n.590-24_590-22delinsGGT
ENST00000613923.4:c.590-24_590-22delinsGGT	ENSP00000481858.1:n.590-24_590-22delinsGGT
NM_001256849.1:c.590-24_590-22delinsGGT , LRG_785t1:c.590-24_590-22delinsGGT	NP_001243778.1:n.590-24_590-22delinsGGT
NM_001308632.1:c.590-24_590-22delinsGGT , LRG_785t2:c.590-24_590-22delinsGGT	NP_001295561.1:n.590-24_590-22delinsGGT
NM_002691.3:c.590-24_590-22delinsGGT	NP_002682.2:n.590-24_590-22delinsGGT
NR_046402.1:n.659-24_659-22delinsGGT
XM_005259008.3:c.590-24_590-22delinsGGT	XP_005259065.1:n.590-24_590-22delinsGGT
XM_011527038.1:c.590-24_590-22delinsGGT	XP_011525340.1:n.590-24_590-22delinsGGT
XM_011527039.1:c.590-24_590-22delinsGGT	XP_011525341.1:n.590-24_590-22delinsGGT
XR_935835.1:n.692-24_692-22delinsGGT
XM_005259008.4:c.590-24_590-22delinsGGT	XP_005259065.1:n.590-24_590-22delinsGGT
XM_017026881.1:c.590-24_590-22delinsGGT	XP_016882370.1:n.590-24_590-22delinsGGT
XM_017026882.2:c.590-24_590-22delinsGGT	XP_016882371.1:n.590-24_590-22delinsGGT
XR_935835.2:n.691-24_691-22delinsGGT
NM_002691.4:c.590-24_590-22delinsGGT MANE Select	NP_002682.2:n.590-24_590-22delinsGGT
NR_046402.2:n.635-24_635-22delinsGGT