Canonical Allele Identifier: CA916082470

Gene: POLD1

Linked Data

• ClinVar Variation Id: 834685
• ClinVar RCV Id: RCV001035422
• dbSNP Id: rs2038699519

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50402655_50402656del , CM000681.2:g.50402655_50402656del	GRCh38
NC_000019.9:g.50905912_50905913del , CM000681.1:g.50905912_50905913del	GRCh37
NC_000019.8:g.55597724_55597725del	NCBI36
NG_033800.1:g.23333_23334del , LRG_785:g.23333_23334del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593887.2:c.884_885del	ENSP00000472607.2:p.Val295GlyfsTer?
ENST00000600746.2:n.1075_1076del
ENST00000644560.2:c.884_885del	ENSP00000495618.2:p.Val295GlyfsTer?
ENST00000687454.1:c.884_885del	ENSP00000510052.1:p.Val295GlyfsTer?
ENST00000440232.7:c.884_885del MANE Select	ENSP00000406046.1:p.Val295GlyfsTer?
ENST00000595904.6:c.884_885del	ENSP00000472445.1:p.Val295GlyfsTer?
ENST00000599857.7:c.884_885del	ENSP00000473052.1:p.Val295GlyfsTer?
ENST00000601098.6:c.884_885del	ENSP00000472600.2:p.Val295GlyfsTer?
ENST00000613923.6:c.884_885del	ENSP00000481858.2:p.Val295GlyfsTer?
ENST00000643407.1:c.884_885del	ENSP00000496078.1:p.Val295GlyfsTer?
ENST00000440232.6:c.884_885del	ENSP00000406046.1:p.Val295GlyfsTer?
ENST00000595904.5:c.884_885del	ENSP00000472445.1:p.Val295GlyfsTer?
ENST00000599857.5:c.884_885del	ENSP00000473052.1:p.Val295GlyfsTer?
ENST00000600746.1:n.989_990del
ENST00000600859.5:c.884_885del	ENSP00000470726.1:p.Val295GlyfsTer?
ENST00000613923.4:c.884_885del	ENSP00000481858.1:p.Val295GlyfsTer?
NM_001256849.1:c.884_885del , LRG_785t1:c.884_885del	NP_001243778.1:p.Val295GlyfsTer?
NM_001308632.1:c.884_885del , LRG_785t2:c.884_885del	NP_001295561.1:p.Val295GlyfsTer?
NM_002691.3:c.884_885del	NP_002682.2:p.Val295GlyfsTer?
NR_046402.1:n.953_954del
XM_005259008.3:c.884_885del	XP_005259065.1:p.Val295GlyfsTer?
XM_011527038.1:c.884_885del	XP_011525340.1:p.Val295GlyfsTer?
XM_011527039.1:c.884_885del	XP_011525341.1:p.Val295GlyfsTer?
XR_935835.1:n.986_987del
XM_005259008.4:c.884_885del	XP_005259065.1:p.Val295GlyfsTer?
XM_017026881.1:c.884_885del	XP_016882370.1:p.Val295GlyfsTer?
XM_017026882.2:c.884_885del	XP_016882371.1:p.Val295GlyfsTer?
XR_935835.2:n.985_986del
NM_002691.4:c.884_885del MANE Select	NP_002682.2:p.Val295GlyfsTer?
NR_046402.2:n.929_930del