Canonical Allele Identifier: CA1139828712

Gene: PARP1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.226363477A= , CM000663.2:g.226363477A=	GRCh38
NC_000001.10:g.226551178A= , CM000663.1:g.226551178A=	GRCh37
NC_000001.9:g.224617801A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366794.10:c.2787-317T= MANE Select	ENSP00000355759.5:n.2787-317T=
ENST00000498787.2:n.4342T=
ENST00000676481.1:n.232-317T=
ENST00000676565.1:n.2559-317T=
ENST00000676685.1:n.4904T=
ENST00000676709.1:n.3477T=
ENST00000677091.1:c.*1469-317T=	ENSP00000504745.1:n.*1469-317T=
ENST00000677189.1:n.840-317T=
ENST00000677203.1:c.2658-317T=	ENSP00000503396.1:n.2658-317T=
ENST00000677374.1:n.4438T=
ENST00000677815.1:n.2679T=
ENST00000677884.1:n.3599-317T=
ENST00000677985.1:n.777-317T=
ENST00000678144.1:c.*1607-317T=	ENSP00000504430.1:n.*1607-317T=
ENST00000678226.1:n.1766-317T=
ENST00000678288.1:n.912-317T=
ENST00000678560.1:c.*2775-317T=	ENSP00000503293.1:n.*2775-317T=
ENST00000678781.1:n.4439-317T=
ENST00000679276.1:n.3943-317T=
ENST00000366794.9:c.2787-317T=	ENSP00000355759.5:n.2787-317T=
ENST00000463968.5:n.431-317T=
ENST00000490921.5:n.2742-317T=
NM_001618.3:c.2787-317T=	NP_001609.2:n.2787-317T=
NM_001618.4:c.2787-317T= MANE Select	NP_001609.2:n.2787-317T=