Canonical Allele Identifier: CA1139895385

Gene: PARP1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.226385663A= , CM000663.2:g.226385663A=	GRCh38
NC_000001.10:g.226573364A= , CM000663.1:g.226573364A=	GRCh37
NC_000001.9:g.224639987A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366794.10:c.852T= MANE Select	ENSP00000355759.5:p.Ala284=
ENST00000676685.1:n.1077T=
ENST00000676709.1:n.1077T=
ENST00000677091.1:c.852T=	ENSP00000504745.1:p.Ala284=
ENST00000677203.1:c.852T=	ENSP00000503396.1:p.Ala284=
ENST00000677374.1:n.1135T=
ENST00000677884.1:n.1664T=
ENST00000678144.1:c.852T=	ENSP00000504430.1:p.Ala284=
ENST00000678560.1:c.*840T=	ENSP00000503293.1:n.*840T=
ENST00000678781.1:n.1077T=
ENST00000679276.1:n.1077T=
ENST00000366794.9:c.852T=	ENSP00000355759.5:p.Ala284=
NM_001618.3:c.852T=	NP_001609.2:p.Ala284=
NM_001618.4:c.852T= MANE Select	NP_001609.2:p.Ala284=