Canonical Allele Identifier: CA2536557201

Gene: POLD1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50401943_50401944insGA , CM000681.2:g.50401943_50401944insGA	GRCh38
NC_000019.9:g.50905200_50905201insGA , CM000681.1:g.50905200_50905201insGA	GRCh37
NC_000019.8:g.55597012_55597013insGA	NCBI36
NG_033800.1:g.22621_22622insGA , LRG_785:g.22621_22622insGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593887.2:c.463+19_463+20insGA	ENSP00000472607.2:n.463+19_463+20insGA
ENST00000600746.2:n.574+19_574+20insGA
ENST00000644560.2:c.463+19_463+20insGA	ENSP00000495618.2:n.463+19_463+20insGA
ENST00000687454.1:c.463+19_463+20insGA	ENSP00000510052.1:n.463+19_463+20insGA
ENST00000440232.7:c.463+19_463+20insGA MANE Select	ENSP00000406046.1:n.463+19_463+20insGA
ENST00000595904.6:c.463+19_463+20insGA	ENSP00000472445.1:n.463+19_463+20insGA
ENST00000599857.7:c.463+19_463+20insGA	ENSP00000473052.1:n.463+19_463+20insGA
ENST00000601098.6:c.463+19_463+20insGA	ENSP00000472600.2:n.463+19_463+20insGA
ENST00000613923.6:c.463+19_463+20insGA	ENSP00000481858.2:n.463+19_463+20insGA
ENST00000643407.1:c.463+19_463+20insGA	ENSP00000496078.1:n.463+19_463+20insGA
ENST00000440232.6:c.463+19_463+20insGA	ENSP00000406046.1:n.463+19_463+20insGA
ENST00000595904.5:c.463+19_463+20insGA	ENSP00000472445.1:n.463+19_463+20insGA
ENST00000599857.5:c.463+19_463+20insGA	ENSP00000473052.1:n.463+19_463+20insGA
ENST00000600746.1:n.488+19_488+20insGA
ENST00000600859.5:c.463+19_463+20insGA	ENSP00000470726.1:n.463+19_463+20insGA
ENST00000601098.5:c.463+19_463+20insGA	ENSP00000472600.1:n.463+19_463+20insGA
ENST00000613923.4:c.463+19_463+20insGA	ENSP00000481858.1:n.463+19_463+20insGA
NM_001256849.1:c.463+19_463+20insGA , LRG_785t1:c.463+19_463+20insGA	NP_001243778.1:n.463+19_463+20insGA
NM_001308632.1:c.463+19_463+20insGA , LRG_785t2:c.463+19_463+20insGA	NP_001295561.1:n.463+19_463+20insGA
NM_002691.3:c.463+19_463+20insGA	NP_002682.2:n.463+19_463+20insGA
NR_046402.1:n.532+19_532+20insGA
XM_005259008.3:c.463+19_463+20insGA	XP_005259065.1:n.463+19_463+20insGA
XM_011527038.1:c.463+19_463+20insGA	XP_011525340.1:n.463+19_463+20insGA
XM_011527039.1:c.463+19_463+20insGA	XP_011525341.1:n.463+19_463+20insGA
XR_935835.1:n.565+19_565+20insGA
XM_005259008.4:c.463+19_463+20insGA	XP_005259065.1:n.463+19_463+20insGA
XM_017026881.1:c.463+19_463+20insGA	XP_016882370.1:n.463+19_463+20insGA
XM_017026882.2:c.463+19_463+20insGA	XP_016882371.1:n.463+19_463+20insGA
XR_935835.2:n.564+19_564+20insGA
NM_002691.4:c.463+19_463+20insGA MANE Select	NP_002682.2:n.463+19_463+20insGA
NR_046402.2:n.508+19_508+20insGA