Canonical Allele Identifier: CA2340886543

Gene: POLD1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50408817_50408820delinsTCTC , CM000681.2:g.50408817_50408820delinsTCTC	GRCh38
NC_000019.9:g.50912074_50912077delinsTCTC , CM000681.1:g.50912074_50912077delinsTCTC	GRCh37
NC_000019.8:g.55603886_55603889delinsTCTC	NCBI36
NG_033800.1:g.29495_29498delinsTCTC , LRG_785:g.29495_29498delinsTCTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593887.2:c.1808_1811delinsTCTC	ENSP00000472607.2:p.Phe603=
ENST00000600746.2:n.1999_2002delinsTCTC
ENST00000644560.2:c.1886_1889delinsTCTC	ENSP00000495618.2:p.Phe629=
ENST00000687454.1:c.1808_1811delinsTCTC	ENSP00000510052.1:p.Phe603=
ENST00000440232.7:c.1808_1811delinsTCTC MANE Select	ENSP00000406046.1:p.Phe603=
ENST00000595904.6:c.1886_1889delinsTCTC	ENSP00000472445.1:p.Phe629=
ENST00000599857.7:c.1808_1811delinsTCTC	ENSP00000473052.1:p.Phe603=
ENST00000601098.6:c.1808_1811delinsTCTC	ENSP00000472600.2:p.Phe603=
ENST00000613923.6:c.1808_1811delinsTCTC	ENSP00000481858.2:p.Phe603=
ENST00000643407.1:c.1808_1811delinsTCTC	ENSP00000496078.1:p.Phe603=
ENST00000644560.1:c.757_760delinsTCTC
ENST00000440232.6:c.1808_1811delinsTCTC	ENSP00000406046.1:p.Phe603=
ENST00000595904.5:c.1886_1889delinsTCTC	ENSP00000472445.1:p.Phe629=
ENST00000596425.1:c.213_216delinsTCTC
ENST00000599857.5:c.1808_1811delinsTCTC	ENSP00000473052.1:p.Phe603=
ENST00000600859.5:c.1808_1811delinsTCTC	ENSP00000470726.1:p.Phe603=
ENST00000613923.4:c.1886_1889delinsTCTC	ENSP00000481858.1:p.Phe629=
NM_001256849.1:c.1808_1811delinsTCTC , LRG_785t1:c.1808_1811delinsTCTC	NP_001243778.1:p.Phe603=
NM_001308632.1:c.1886_1889delinsTCTC , LRG_785t2:c.1886_1889delinsTCTC	NP_001295561.1:p.Phe629=
NM_002691.3:c.1808_1811delinsTCTC	NP_002682.2:p.Phe603=
NR_046402.1:n.1877_1880delinsTCTC
XM_005259008.3:c.1808_1811delinsTCTC	XP_005259065.1:p.Phe603=
XM_011527038.1:c.1808_1811delinsTCTC	XP_011525340.1:p.Phe603=
XM_011527039.1:c.1808_1811delinsTCTC	XP_011525341.1:p.Phe603=
XR_935835.1:n.1910_1913delinsTCTC
XM_005259008.4:c.1808_1811delinsTCTC	XP_005259065.1:p.Phe603=
XM_017026881.1:c.1808_1811delinsTCTC	XP_016882370.1:p.Phe603=
XM_017026882.2:c.1808_1811delinsTCTC	XP_016882371.1:p.Phe603=
XR_935835.2:n.1909_1912delinsTCTC
NM_002691.4:c.1808_1811delinsTCTC MANE Select	NP_002682.2:p.Phe603=
NR_046402.2:n.1853_1856delinsTCTC