Canonical Allele Identifier: CA2580600466

Gene: POLD3

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.74634505T>C , CM000673.2:g.74634505T>C	GRCh38
NC_000011.9:g.74345550T>C , CM000673.1:g.74345550T>C	GRCh37
NC_000011.8:g.74023198T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263681.7:c.1007-78T>C MANE Select	ENSP00000263681.2:n.1007-78T>C
ENST00000263681.6:c.1007-78T>C	ENSP00000263681.2:n.1007-78T>C
ENST00000524752.1:c.178-78T>C
ENST00000527458.5:c.890-78T>C	ENSP00000432951.1:n.890-78T>C
ENST00000530163.1:n.462-78T>C
ENST00000532497.5:c.689-78T>C	ENSP00000436018.1:n.689-78T>C
NM_006591.2:c.1007-78T>C	NP_006582.1:n.1007-78T>C
NR_046409.1:n.1033-78T>C
NR_046410.1:n.1380-78T>C
XM_005273716.1:c.1007-78T>C	XP_005273773.1:n.1007-78T>C
XM_011544734.1:c.953-78T>C	XP_011543036.1:n.953-78T>C
NM_001363597.1:c.890-78T>C	NP_001350526.1:n.890-78T>C
XM_011544734.3:c.953-78T>C	XP_011543036.1:n.953-78T>C
NM_001363597.2:c.890-78T>C	NP_001350526.1:n.890-78T>C
NM_006591.3:c.1007-78T>C MANE Select	NP_006582.1:n.1007-78T>C
NR_046409.2:n.981-78T>C
NR_046410.2:n.1403-78T>C