Canonical Allele Identifier: CA2340886929

Gene: POLD1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50409587C= , CM000681.2:g.50409587C=	GRCh38
NC_000019.9:g.50912844C= , CM000681.1:g.50912844C=	GRCh37
NC_000019.8:g.55604656C=	NCBI36
NG_033800.1:g.30265C= , LRG_785:g.30265C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593887.2:c.2075C=	ENSP00000472607.2:p.Ala692=
ENST00000600746.2:n.2266C=
ENST00000644560.2:c.2153C=	ENSP00000495618.2:p.Ala718=
ENST00000687454.1:c.2075C=	ENSP00000510052.1:p.Ala692=
ENST00000440232.7:c.2075C= MANE Select	ENSP00000406046.1:p.Ala692=
ENST00000595904.6:c.2153C=	ENSP00000472445.1:p.Ala718=
ENST00000599857.7:c.2075C=	ENSP00000473052.1:p.Ala692=
ENST00000601098.6:c.2075C=	ENSP00000472600.2:p.Ala692=
ENST00000613923.6:c.2075C=	ENSP00000481858.2:p.Ala692=
ENST00000643407.1:c.2075C=	ENSP00000496078.1:p.Ala692=
ENST00000644560.1:c.1024C=
ENST00000440232.6:c.2075C=	ENSP00000406046.1:p.Ala692=
ENST00000595904.5:c.2153C=	ENSP00000472445.1:p.Ala718=
ENST00000596425.1:c.480C=
ENST00000599857.5:c.2075C=	ENSP00000473052.1:p.Ala692=
ENST00000600859.5:c.2075C=	ENSP00000470726.1:p.Ala692=
ENST00000613923.4:c.2153C=	ENSP00000481858.1:p.Ala718=
NM_001256849.1:c.2075C= , LRG_785t1:c.2075C=	NP_001243778.1:p.Ala692=
NM_001308632.1:c.2153C= , LRG_785t2:c.2153C=	NP_001295561.1:p.Ala718=
NM_002691.3:c.2075C=	NP_002682.2:p.Ala692=
NR_046402.1:n.2144C=
XM_005259008.3:c.2075C=	XP_005259065.1:p.Ala692=
XM_011527038.1:c.2075C=	XP_011525340.1:p.Ala692=
XM_011527039.1:c.2075C=	XP_011525341.1:p.Ala692=
XR_935835.1:n.2177C=
XM_005259008.4:c.2075C=	XP_005259065.1:p.Ala692=
XM_017026881.1:c.2075C=	XP_016882370.1:p.Ala692=
XM_017026882.2:c.2075C=	XP_016882371.1:p.Ala692=
XR_935835.2:n.2176C=
NM_002691.4:c.2075C= MANE Select	NP_002682.2:p.Ala692=
NR_046402.2:n.2120C=