Canonical Allele Identifier: CA1545887941

Gene: PARP8

Linked Data

• dbSNP Id: rs12055210

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.50693867A>T , CM000667.2:g.50693867A>T	GRCh38
NC_000005.9:g.49989701A>T , CM000667.1:g.49989701A>T	GRCh37
NC_000005.8:g.50025458A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000281631.10:c.146+25742A>T MANE Select	ENSP00000281631.4:n.146+25742A>T
ENST00000515175.6:c.269+25742A>T	ENSP00000423133.2:n.269+25742A>T
ENST00000281631.9:c.146+25742A>T	ENSP00000281631.4:n.146+25742A>T
ENST00000502524.5:c.146+25742A>T	ENSP00000426243.1:n.146+25742A>T
ENST00000503046.5:c.146+25742A>T	ENSP00000421708.1:n.146+25742A>T
ENST00000503193.5:c.91+26681A>T	ENSP00000424916.1:n.91+26681A>T
ENST00000503561.7:n.233+25742A>T
ENST00000503665.5:c.146+25742A>T	ENSP00000427138.1:n.146+25742A>T
ENST00000503707.6:c.146+25742A>T	ENSP00000426679.2:n.146+25742A>T
ENST00000503750.3:c.-525+25742A>T	ENSP00000440851.2:n.-525+25742A>T
ENST00000503790.6:n.328+25742A>T
ENST00000503888.5:c.91+26681A>T	ENSP00000421503.1:n.91+26681A>T
ENST00000505180.5:n.242+25742A>T
ENST00000505554.5:c.83+25742A>T	ENSP00000423946.1:n.83+25742A>T
ENST00000505697.6:c.146+25742A>T	ENSP00000422217.2:n.146+25742A>T
ENST00000507812.5:c.146+25742A>T	ENSP00000422183.1:n.146+25742A>T
ENST00000510303.6:c.146+25742A>T	ENSP00000422288.2:n.146+25742A>T
ENST00000511363.6:n.328+25742A>T
ENST00000513738.5:c.146+25742A>T	ENSP00000422355.1:n.146+25742A>T
ENST00000514067.6:c.146+25742A>T	ENSP00000424814.2:n.146+25742A>T
ENST00000514342.6:c.-596+25742A>T	ENSP00000439022.1:n.-596+25742A>T
ENST00000515166.5:c.146+25742A>T	ENSP00000424485.1:n.146+25742A>T
ENST00000515175.5:c.146+25742A>T	ENSP00000423133.1:n.146+25742A>T
NM_001178055.1:c.146+25742A>T	NP_001171526.1:n.146+25742A>T
NM_001178056.1:c.146+25742A>T	NP_001171527.1:n.146+25742A>T
NM_024615.3:c.146+25742A>T	NP_078891.2:n.146+25742A>T
XM_005248596.3:c.269+25742A>T	XP_005248653.1:n.269+25742A>T
XM_011543631.1:c.146+25742A>T	XP_011541933.1:n.146+25742A>T
XM_011543632.1:c.269+25742A>T	XP_011541934.1:n.269+25742A>T
XM_011543633.1:c.269+25742A>T	XP_011541935.1:n.269+25742A>T
XM_011543634.1:c.-573+25742A>T	XP_011541936.1:n.-573+25742A>T
XM_011543635.1:c.-132+25742A>T	XP_011541937.1:n.-132+25742A>T
XM_011543636.1:c.-132+25742A>T	XP_011541938.1:n.-132+25742A>T
XM_011543637.1:c.-132+26681A>T	XP_011541939.1:n.-132+26681A>T
XM_011543638.1:c.269+25742A>T	XP_011541940.1:n.269+25742A>T
XM_011543639.1:c.269+25742A>T	XP_011541941.1:n.269+25742A>T
XM_011543640.1:c.-285+25742A>T	XP_011541942.1:n.-285+25742A>T
XM_011543641.1:c.-285+25742A>T	XP_011541943.1:n.-285+25742A>T
XM_011543642.1:c.-214+25742A>T	XP_011541944.1:n.-214+25742A>T
XM_011543643.1:c.-655+25742A>T	XP_011541945.1:n.-655+25742A>T
XM_011543644.1:c.269+25742A>T	XP_011541946.1:n.269+25742A>T
XM_011543645.1:c.-596+26681A>T	XP_011541947.1:n.-596+26681A>T
NM_001331028.1:c.83+25742A>T	NP_001317957.1:n.83+25742A>T
XM_005248596.5:c.269+25742A>T	XP_005248653.1:n.269+25742A>T
XM_011543631.3:c.146+25742A>T	XP_011541933.1:n.146+25742A>T
XM_011543632.3:c.146+25742A>T	XP_011541934.2:n.146+25742A>T
XM_011543633.3:c.146+25742A>T	XP_011541935.2:n.146+25742A>T
XM_011543634.2:c.-573+25742A>T	XP_011541936.1:n.-573+25742A>T
XM_011543635.2:c.-132+25742A>T	XP_011541937.1:n.-132+25742A>T
XM_011543636.2:c.-132+25742A>T	XP_011541938.1:n.-132+25742A>T
XM_011543640.3:c.-285+25742A>T	XP_011541942.1:n.-285+25742A>T
XM_011543641.2:c.-285+25742A>T	XP_011541943.1:n.-285+25742A>T
XM_011543642.2:c.-214+25742A>T	XP_011541944.1:n.-214+25742A>T
XM_011543643.2:c.-655+25742A>T	XP_011541945.1:n.-655+25742A>T
XM_017009851.1:c.-525+25742A>T	XP_016865340.1:n.-525+25742A>T
XM_024446206.1:c.-214+27798A>T	XP_024301974.1:n.-214+27798A>T
NM_024615.4:c.146+25742A>T MANE Select	NP_078891.2:n.146+25742A>T
NM_001178055.2:c.146+25742A>T	NP_001171526.1:n.146+25742A>T
NM_001178056.2:c.146+25742A>T	NP_001171527.1:n.146+25742A>T
NM_001331028.2:c.83+25742A>T	NP_001317957.1:n.83+25742A>T