Canonical Allele Identifier: CA406984490
Gene: POLD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50414813A>T , CM000681.2:g.50414813A>T GRCh38
NC_000019.9:g.50918070A>T , CM000681.1:g.50918070A>T GRCh37
NC_000019.8:g.55609882A>T NCBI36
NG_033800.1:g.35491A>T , LRG_785:g.35491A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000593887.2:c.2389-2A>T ENSP00000472607.2:n.2389-2A>T
ENST00000600746.2:n.2580-2A>T
ENST00000644560.2:c.2395-2A>T ENSP00000495618.2:n.2395-2A>T
ENST00000687454.1:c.2389-2A>T ENSP00000510052.1:n.2389-2A>T
ENST00000440232.7:c.2389-2A>T MANE Select ENSP00000406046.1:n.2389-2A>T
ENST00000595904.6:c.2467-2A>T ENSP00000472445.1:n.2467-2A>T
ENST00000599857.7:c.2389-2A>T ENSP00000473052.1:n.2389-2A>T
ENST00000601098.6:c.2389-2A>T ENSP00000472600.2:n.2389-2A>T
ENST00000613923.6:c.2317-2A>T ENSP00000481858.2:n.2317-2A>T
ENST00000643407.1:c.*176-2A>T ENSP00000496078.1:n.*176-2A>T
ENST00000644560.1:c.1266-2A>T
ENST00000440232.6:c.2389-2A>T ENSP00000406046.1:n.2389-2A>T
ENST00000593407.5:c.158-2A>T
ENST00000593981.1:c.15-2A>T
ENST00000595904.5:c.2467-2A>T ENSP00000472445.1:n.2467-2A>T
ENST00000599857.5:c.2389-2A>T ENSP00000473052.1:n.2389-2A>T
ENST00000600859.5:c.2389-2A>T ENSP00000470726.1:n.2389-2A>T
ENST00000613923.4:c.2467-2A>T ENSP00000481858.1:n.2467-2A>T
NM_001256849.1:c.2389-2A>T , LRG_785t1:c.2389-2A>T NP_001243778.1:n.2389-2A>T
NM_001308632.1:c.2467-2A>T , LRG_785t2:c.2467-2A>T NP_001295561.1:n.2467-2A>T
NM_002691.3:c.2389-2A>T NP_002682.2:n.2389-2A>T
NR_046402.1:n.2458-2A>T
XM_005259008.3:c.2317-2A>T XP_005259065.1:n.2317-2A>T
XM_011527038.1:c.2389-2A>T XP_011525340.1:n.2389-2A>T
XM_011527039.1:c.2389-2A>T XP_011525341.1:n.2389-2A>T
XM_005259008.4:c.2317-2A>T XP_005259065.1:n.2317-2A>T
XM_017026881.1:c.2389-2A>T XP_016882370.1:n.2389-2A>T
XM_017026882.2:c.2317-2A>T XP_016882371.1:n.2317-2A>T
NM_002691.4:c.2389-2A>T MANE Select NP_002682.2:n.2389-2A>T
NR_046402.2:n.2434-2A>T