Canonical Allele Identifier: CA1422362

Gene: PARP1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.226363128T>C , CM000663.2:g.226363128T>C	GRCh38
NC_000001.10:g.226550829T>C , CM000663.1:g.226550829T>C	GRCh37
NC_000001.9:g.224617452T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001618.4:c.2819A>G MANE Select	NP_001609.2:p.Lys940Arg
ENST00000366794.10:c.2819A>G MANE Select	ENSP00000355759.5:p.Lys940Arg
NM_001618.3:c.2819A>G	NP_001609.2:p.Lys940Arg
ENST00000366794.9:c.2819A>G	ENSP00000355759.5:p.Lys940Arg
ENST00000463968.5:n.463A>G
ENST00000468608.1:n.33A>G
ENST00000490921.5:n.2774A>G
ENST00000498787.2:n.4691A>G
ENST00000676481.1:n.264A>G
ENST00000676565.1:n.2591A>G
ENST00000676685.1:n.5253A>G
ENST00000676709.1:n.3826A>G
ENST00000677091.1:c.*1501A>G	ENSP00000504745.1:n.*1501A>G
ENST00000677189.1:n.872A>G
ENST00000677203.1:c.2690A>G	ENSP00000503396.1:p.Lys897Arg
ENST00000677374.1:n.4787A>G
ENST00000677815.1:n.3028A>G
ENST00000677884.1:n.3631A>G
ENST00000677985.1:n.809A>G
ENST00000678144.1:c.*1639A>G	ENSP00000504430.1:n.*1639A>G
ENST00000678226.1:n.1798A>G
ENST00000678288.1:n.944A>G
ENST00000678560.1:c.*2807A>G	ENSP00000503293.1:n.*2807A>G
ENST00000678781.1:n.4471A>G
ENST00000679276.1:n.3975A>G