Canonical Allele Identifier: CA345034703

Gene: PARP1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.226367601A>T , CM000663.2:g.226367601A>T	GRCh38
NC_000001.10:g.226555302A>T , CM000663.1:g.226555302A>T	GRCh37
NC_000001.9:g.224621925A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366794.10:c.2285T>A MANE Select	ENSP00000355759.5:p.Val762Glu
ENST00000498787.2:n.2444T>A
ENST00000676565.1:n.2057T>A
ENST00000676685.1:n.2510T>A
ENST00000676709.1:n.2510T>A
ENST00000677091.1:c.*967T>A	ENSP00000504745.1:n.*967T>A
ENST00000677189.1:n.338T>A
ENST00000677203.1:c.2156T>A	ENSP00000503396.1:p.Val719Glu
ENST00000677374.1:n.3471T>A
ENST00000677884.1:n.3097T>A
ENST00000677985.1:n.275T>A
ENST00000678144.1:c.*1105T>A	ENSP00000504430.1:n.*1105T>A
ENST00000678226.1:n.1264T>A
ENST00000678288.1:n.410T>A
ENST00000678560.1:c.*2273T>A	ENSP00000503293.1:n.*2273T>A
ENST00000678781.1:n.2510T>A
ENST00000679276.1:n.2510T>A
ENST00000366794.9:c.2285T>A	ENSP00000355759.5:p.Val762Glu
ENST00000490921.5:n.813T>A
ENST00000498787.1:n.341T>A
NM_001618.3:c.2285T>A	NP_001609.2:p.Val762Glu
NM_001618.4:c.2285T>A MANE Select	NP_001609.2:p.Val762Glu