Canonical Allele Identifier: CA406981938

Gene: POLD1

Linked Data

• ClinVar Variation Id: 2810523
• ClinVar RCV Id: RCV003641440
• gnomAD v4: 19-50408789-T-G
• MyVariant Identifiers: chr19:g.50912046T>G (hg19) ; chr19:g.50408789T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50408789T>G , CM000681.2:g.50408789T>G	GRCh38
NC_000019.9:g.50912046T>G , CM000681.1:g.50912046T>G	GRCh37
NC_000019.8:g.55603858T>G	NCBI36
NG_033800.1:g.29467T>G , LRG_785:g.29467T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593887.2:c.1780T>G	ENSP00000472607.2:p.Tyr594Asp
ENST00000600746.2:n.1971T>G
ENST00000644560.2:c.1858T>G	ENSP00000495618.2:p.Tyr620Asp
ENST00000687454.1:c.1780T>G	ENSP00000510052.1:p.Tyr594Asp
ENST00000440232.7:c.1780T>G MANE Select	ENSP00000406046.1:p.Tyr594Asp
ENST00000595904.6:c.1858T>G	ENSP00000472445.1:p.Tyr620Asp
ENST00000599857.7:c.1780T>G	ENSP00000473052.1:p.Tyr594Asp
ENST00000601098.6:c.1780T>G	ENSP00000472600.2:p.Tyr594Asp
ENST00000613923.6:c.1780T>G	ENSP00000481858.2:p.Tyr594Asp
ENST00000643407.1:c.1780T>G	ENSP00000496078.1:p.Tyr594Asp
ENST00000644560.1:c.729T>G
ENST00000440232.6:c.1780T>G	ENSP00000406046.1:p.Tyr594Asp
ENST00000595904.5:c.1858T>G	ENSP00000472445.1:p.Tyr620Asp
ENST00000596425.1:c.185T>G
ENST00000599857.5:c.1780T>G	ENSP00000473052.1:p.Tyr594Asp
ENST00000600859.5:c.1780T>G	ENSP00000470726.1:p.Tyr594Asp
ENST00000613923.4:c.1858T>G	ENSP00000481858.1:p.Tyr620Asp
NM_001256849.1:c.1780T>G , LRG_785t1:c.1780T>G	NP_001243778.1:p.Tyr594Asp
NM_001308632.1:c.1858T>G , LRG_785t2:c.1858T>G	NP_001295561.1:p.Tyr620Asp
NM_002691.3:c.1780T>G	NP_002682.2:p.Tyr594Asp
NR_046402.1:n.1849T>G
XM_005259008.3:c.1780T>G	XP_005259065.1:p.Tyr594Asp
XM_011527038.1:c.1780T>G	XP_011525340.1:p.Tyr594Asp
XM_011527039.1:c.1780T>G	XP_011525341.1:p.Tyr594Asp
XR_935835.1:n.1882T>G
XM_005259008.4:c.1780T>G	XP_005259065.1:p.Tyr594Asp
XM_017026881.1:c.1780T>G	XP_016882370.1:p.Tyr594Asp
XM_017026882.2:c.1780T>G	XP_016882371.1:p.Tyr594Asp
XR_935835.2:n.1881T>G
NM_002691.4:c.1780T>G MANE Select	NP_002682.2:p.Tyr594Asp
NR_046402.2:n.1825T>G