Canonical Allele Identifier: CA2340882457

Gene: POLD1

Linked Data

• ClinVar Variation Id: 949585
• ClinVar RCV Id: RCV001221075 ; RCV001819913
• dbSNP Id: rs2038649098
• gnomAD v4: 19-50401866-CTCTG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50401871_50401874del , CM000681.2:g.50401871_50401874del	GRCh38
NC_000019.9:g.50905128_50905131del , CM000681.1:g.50905128_50905131del	GRCh37
NC_000019.8:g.55596940_55596943del	NCBI36
NG_033800.1:g.22549_22552del , LRG_785:g.22549_22552del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593887.2:c.410_413del	ENSP00000472607.2:p.Val137AlafsTer?
ENST00000600746.2:n.521_524del
ENST00000644560.2:c.410_413del	ENSP00000495618.2:p.Val137AlafsTer?
ENST00000687454.1:c.410_413del	ENSP00000510052.1:p.Val137AlafsTer?
ENST00000440232.7:c.410_413del MANE Select	ENSP00000406046.1:p.Val137AlafsTer?
ENST00000595904.6:c.410_413del	ENSP00000472445.1:p.Val137AlafsTer?
ENST00000599857.7:c.410_413del	ENSP00000473052.1:p.Val137AlafsTer?
ENST00000601098.6:c.410_413del	ENSP00000472600.2:p.Val137AlafsTer?
ENST00000613923.6:c.410_413del	ENSP00000481858.2:p.Val137AlafsTer?
ENST00000643407.1:c.410_413del	ENSP00000496078.1:p.Val137AlafsTer?
ENST00000440232.6:c.410_413del	ENSP00000406046.1:p.Val137AlafsTer?
ENST00000595904.5:c.410_413del	ENSP00000472445.1:p.Val137AlafsTer?
ENST00000599857.5:c.410_413del	ENSP00000473052.1:p.Val137AlafsTer?
ENST00000600746.1:n.435_438del
ENST00000600859.5:c.410_413del	ENSP00000470726.1:p.Val137AlafsTer?
ENST00000601098.5:c.410_413del	ENSP00000472600.1:p.Val137AlafsTer?
ENST00000613923.4:c.410_413del	ENSP00000481858.1:p.Val137AlafsTer?
NM_001256849.1:c.410_413del , LRG_785t1:c.410_413del	NP_001243778.1:p.Val137AlafsTer?
NM_001308632.1:c.410_413del , LRG_785t2:c.410_413del	NP_001295561.1:p.Val137AlafsTer?
NM_002691.3:c.410_413del	NP_002682.2:p.Val137AlafsTer?
NR_046402.1:n.479_482del
XM_005259008.3:c.410_413del	XP_005259065.1:p.Val137AlafsTer?
XM_011527038.1:c.410_413del	XP_011525340.1:p.Val137AlafsTer?
XM_011527039.1:c.410_413del	XP_011525341.1:p.Val137AlafsTer?
XR_935835.1:n.512_515del
XM_005259008.4:c.410_413del	XP_005259065.1:p.Val137AlafsTer?
XM_017026881.1:c.410_413del	XP_016882370.1:p.Val137AlafsTer?
XM_017026882.2:c.410_413del	XP_016882371.1:p.Val137AlafsTer?
XR_935835.2:n.511_514del
NM_002691.4:c.410_413del MANE Select	NP_002682.2:p.Val137AlafsTer?
NR_046402.2:n.455_458del