Canonical Allele Identifier: CA406982149

Gene: POLD1

Linked Data

• dbSNP Id: rs1297363872
• MyVariant Identifiers: chr19:g.50912148C>G (hg19) ; chr19:g.50408891C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50408891C>G , CM000681.2:g.50408891C>G	GRCh38
NC_000019.9:g.50912148C>G , CM000681.1:g.50912148C>G	GRCh37
NC_000019.8:g.55603960C>G	NCBI36
NG_033800.1:g.29569C>G , LRG_785:g.29569C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593887.2:c.1882C>G	ENSP00000472607.2:p.Gln628Glu
ENST00000600746.2:n.2073C>G
ENST00000644560.2:c.1960C>G	ENSP00000495618.2:p.Gln654Glu
ENST00000687454.1:c.1882C>G	ENSP00000510052.1:p.Gln628Glu
ENST00000440232.7:c.1882C>G MANE Select	ENSP00000406046.1:p.Gln628Glu
ENST00000595904.6:c.1960C>G	ENSP00000472445.1:p.Gln654Glu
ENST00000599857.7:c.1882C>G	ENSP00000473052.1:p.Gln628Glu
ENST00000601098.6:c.1882C>G	ENSP00000472600.2:p.Gln628Glu
ENST00000613923.6:c.1882C>G	ENSP00000481858.2:p.Gln628Glu
ENST00000643407.1:c.1882C>G	ENSP00000496078.1:p.Gln628Glu
ENST00000644560.1:c.831C>G
ENST00000440232.6:c.1882C>G	ENSP00000406046.1:p.Gln628Glu
ENST00000595904.5:c.1960C>G	ENSP00000472445.1:p.Gln654Glu
ENST00000596425.1:c.287C>G
ENST00000599857.5:c.1882C>G	ENSP00000473052.1:p.Gln628Glu
ENST00000600859.5:c.1882C>G	ENSP00000470726.1:p.Gln628Glu
ENST00000613923.4:c.1960C>G	ENSP00000481858.1:p.Gln654Glu
NM_001256849.1:c.1882C>G , LRG_785t1:c.1882C>G	NP_001243778.1:p.Gln628Glu
NM_001308632.1:c.1960C>G , LRG_785t2:c.1960C>G	NP_001295561.1:p.Gln654Glu
NM_002691.3:c.1882C>G	NP_002682.2:p.Gln628Glu
NR_046402.1:n.1951C>G
XM_005259008.3:c.1882C>G	XP_005259065.1:p.Gln628Glu
XM_011527038.1:c.1882C>G	XP_011525340.1:p.Gln628Glu
XM_011527039.1:c.1882C>G	XP_011525341.1:p.Gln628Glu
XR_935835.1:n.1984C>G
XM_005259008.4:c.1882C>G	XP_005259065.1:p.Gln628Glu
XM_017026881.1:c.1882C>G	XP_016882370.1:p.Gln628Glu
XM_017026882.2:c.1882C>G	XP_016882371.1:p.Gln628Glu
XR_935835.2:n.1983C>G
NM_002691.4:c.1882C>G MANE Select	NP_002682.2:p.Gln628Glu
NR_046402.2:n.1927C>G