Canonical Allele Identifier: CA2340885449

Gene: POLD1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50406921_50406924delinsTCTC , CM000681.2:g.50406921_50406924delinsTCTC	GRCh38
NC_000019.9:g.50910178_50910181delinsTCTC , CM000681.1:g.50910178_50910181delinsTCTC	GRCh37
NC_000019.8:g.55601990_55601993delinsTCTC	NCBI36
NG_033800.1:g.27599_27602delinsTCTC , LRG_785:g.27599_27602delinsTCTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593887.2:c.1495-62_1495-59delinsTCTC	ENSP00000472607.2:n.1495-62_1495-59delinsTCTC
ENST00000600746.2:n.1686-62_1686-59delinsTCTC
ENST00000644560.2:c.1495-62_1495-59delinsTCTC	ENSP00000495618.2:n.1495-62_1495-59delinsTCTC
ENST00000687454.1:c.1495-62_1495-59delinsTCTC	ENSP00000510052.1:n.1495-62_1495-59delinsTCTC
ENST00000440232.7:c.1495-62_1495-59delinsTCTC MANE Select	ENSP00000406046.1:n.1495-62_1495-59delinsTCTC
ENST00000595904.6:c.1495-62_1495-59delinsTCTC	ENSP00000472445.1:n.1495-62_1495-59delinsTCTC
ENST00000599857.7:c.1495-62_1495-59delinsTCTC	ENSP00000473052.1:n.1495-62_1495-59delinsTCTC
ENST00000601098.6:c.1495-62_1495-59delinsTCTC	ENSP00000472600.2:n.1495-62_1495-59delinsTCTC
ENST00000613923.6:c.1495-62_1495-59delinsTCTC	ENSP00000481858.2:n.1495-62_1495-59delinsTCTC
ENST00000643407.1:c.1495-62_1495-59delinsTCTC	ENSP00000496078.1:n.1495-62_1495-59delinsTCTC
ENST00000644560.1:c.366-62_366-59delinsTCTC
ENST00000440232.6:c.1495-62_1495-59delinsTCTC	ENSP00000406046.1:n.1495-62_1495-59delinsTCTC
ENST00000595904.5:c.1495-62_1495-59delinsTCTC	ENSP00000472445.1:n.1495-62_1495-59delinsTCTC
ENST00000599857.5:c.1495-62_1495-59delinsTCTC	ENSP00000473052.1:n.1495-62_1495-59delinsTCTC
ENST00000600859.5:c.1495-62_1495-59delinsTCTC	ENSP00000470726.1:n.1495-62_1495-59delinsTCTC
ENST00000613923.4:c.1495-62_1495-59delinsTCTC	ENSP00000481858.1:n.1495-62_1495-59delinsTCTC
NM_001256849.1:c.1495-62_1495-59delinsTCTC , LRG_785t1:c.1495-62_1495-59delinsTCTC	NP_001243778.1:n.1495-62_1495-59delinsTCTC
NM_001308632.1:c.1495-62_1495-59delinsTCTC , LRG_785t2:c.1495-62_1495-59delinsTCTC	NP_001295561.1:n.1495-62_1495-59delinsTCTC
NM_002691.3:c.1495-62_1495-59delinsTCTC	NP_002682.2:n.1495-62_1495-59delinsTCTC
NR_046402.1:n.1564-62_1564-59delinsTCTC
XM_005259008.3:c.1495-62_1495-59delinsTCTC	XP_005259065.1:n.1495-62_1495-59delinsTCTC
XM_011527038.1:c.1495-62_1495-59delinsTCTC	XP_011525340.1:n.1495-62_1495-59delinsTCTC
XM_011527039.1:c.1495-62_1495-59delinsTCTC	XP_011525341.1:n.1495-62_1495-59delinsTCTC
XR_935835.1:n.1597-62_1597-59delinsTCTC
XM_005259008.4:c.1495-62_1495-59delinsTCTC	XP_005259065.1:n.1495-62_1495-59delinsTCTC
XM_017026881.1:c.1495-62_1495-59delinsTCTC	XP_016882370.1:n.1495-62_1495-59delinsTCTC
XM_017026882.2:c.1495-62_1495-59delinsTCTC	XP_016882371.1:n.1495-62_1495-59delinsTCTC
XR_935835.2:n.1596-62_1596-59delinsTCTC
NM_002691.4:c.1495-62_1495-59delinsTCTC MANE Select	NP_002682.2:n.1495-62_1495-59delinsTCTC
NR_046402.2:n.1540-62_1540-59delinsTCTC