Canonical Allele Identifier: CA633685713

Gene: POLD1

Linked Data

• dbSNP Id: rs1568643334
• gnomAD v2: 19-50921087-C-CCCTGCT
• gnomAD v4: 19-50417830-C-CCCTGCT
• MyVariant Identifiers: chr19:g.50921087_50921088insCCTGCT (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50417832_50417833insTGCTCC , CM000681.2:g.50417832_50417833insTGCTCC	GRCh38
NC_000019.9:g.50921089_50921090insTGCTCC , CM000681.1:g.50921089_50921090insTGCTCC	GRCh37
NC_000019.8:g.55612901_55612902insTGCTCC	NCBI36
NG_033800.1:g.38510_38511insTGCTCC , LRG_785:g.38510_38511insTGCTCC

Transcript Alleles

HGVS	Amino-acid change
ENST00000593887.2:c.3219-10_3219-9insTGCTCC	ENSP00000472607.2:n.3219-10_3219-9insTGCT...
ENST00000600746.2:n.3410-10_3410-9insTGCTCC
ENST00000644560.2:c.3225-10_3225-9insTGCTCC	ENSP00000495618.2:n.3225-10_3225-9insTGCT...
ENST00000687454.1:c.3219-10_3219-9insTGCTCC	ENSP00000510052.1:n.3219-10_3219-9insTGCT...
ENST00000440232.7:c.3219-10_3219-9insTGCTCC MANE Select	ENSP00000406046.1:n.3219-10_3219-9insTGCT...
ENST00000595904.6:c.3297-10_3297-9insTGCTCC	ENSP00000472445.1:n.3297-10_3297-9insTGCT...
ENST00000599857.7:c.3219-10_3219-9insTGCTCC	ENSP00000473052.1:n.3219-10_3219-9insTGCT...
ENST00000601098.6:c.3219-10_3219-9insTGCTCC	ENSP00000472600.2:n.3219-10_3219-9insTGCT...
ENST00000613923.6:c.3147-10_3147-9insTGCTCC	ENSP00000481858.2:n.3147-10_3147-9insTGCT...
ENST00000440232.6:c.3219-10_3219-9insTGCTCC	ENSP00000406046.1:n.3219-10_3219-9insTGCT...
ENST00000593981.1:c.792-10_792-9insTGCTCC
ENST00000595904.5:c.3297-10_3297-9insTGCTCC	ENSP00000472445.1:n.3297-10_3297-9insTGCT...
ENST00000596221.1:n.244-10_244-9insTGCTCC
ENST00000597963.5:n.563-10_563-9insTGCTCC
ENST00000599632.1:c.426+563_426+564insTGCTCC
ENST00000599857.5:c.3219-10_3219-9insTGCTCC	ENSP00000473052.1:n.3219-10_3219-9insTGCT...
ENST00000600859.5:c.*86-10_*86-9insTGCTCC	ENSP00000470726.1:n.*86-10_*86-9insTGCTCC...
ENST00000613923.4:c.3297-10_3297-9insTGCTCC	ENSP00000481858.1:n.3297-10_3297-9insTGCT...
NM_001256849.1:c.3219-10_3219-9insTGCTCC , LRG_785t1:c.3219-10_3219-9insTGCTCC	NP_001243778.1:n.3219-10_3219-9insTGCTCC
NM_001308632.1:c.3297-10_3297-9insTGCTCC , LRG_785t2:c.3297-10_3297-9insTGCTCC	NP_001295561.1:n.3297-10_3297-9insTGCTCC
NM_002691.3:c.3219-10_3219-9insTGCTCC	NP_002682.2:n.3219-10_3219-9insTGCTCC
NR_046402.1:n.3185-10_3185-9insTGCTCC
XM_005259008.3:c.3147-10_3147-9insTGCTCC	XP_005259065.1:n.3147-10_3147-9insTGCTCC
XM_011527038.1:c.3219-10_3219-9insTGCTCC	XP_011525340.1:n.3219-10_3219-9insTGCTCC
XM_011527039.1:c.3219-10_3219-9insTGCTCC	XP_011525341.1:n.3219-10_3219-9insTGCTCC
XM_005259008.4:c.3147-10_3147-9insTGCTCC	XP_005259065.1:n.3147-10_3147-9insTGCTCC
XM_017026881.1:c.3219-10_3219-9insTGCTCC	XP_016882370.1:n.3219-10_3219-9insTGCTCC
XM_017026882.2:c.3147-10_3147-9insTGCTCC	XP_016882371.1:n.3147-10_3147-9insTGCTCC
NM_002691.4:c.3219-10_3219-9insTGCTCC MANE Select	NP_002682.2:n.3219-10_3219-9insTGCTCC
NR_046402.2:n.3161-10_3161-9insTGCTCC