Canonical Allele Identifier: CA2650767384

Gene: PARP1

Linked Data

• gnomAD v4: 1-226377050-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.226377050A>G , CM000663.2:g.226377050A>G	GRCh38
NC_000001.10:g.226564751A>G , CM000663.1:g.226564751A>G	GRCh37
NC_000001.9:g.224631374A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366794.10:c.1941+58T>C MANE Select	ENSP00000355759.5:n.1941+58T>C
ENST00000676685.1:n.2166+58T>C
ENST00000676709.1:n.2166+58T>C
ENST00000677091.1:c.*623+58T>C	ENSP00000504745.1:n.*623+58T>C
ENST00000677203.1:c.1941+58T>C	ENSP00000503396.1:n.1941+58T>C
ENST00000677374.1:n.3127+58T>C
ENST00000677884.1:n.2753+58T>C
ENST00000678144.1:c.*761+58T>C	ENSP00000504430.1:n.*761+58T>C
ENST00000678226.1:n.920+58T>C
ENST00000678560.1:c.*1929+58T>C	ENSP00000503293.1:n.*1929+58T>C
ENST00000678781.1:n.2166+58T>C
ENST00000679276.1:n.2166+58T>C
ENST00000366794.9:c.1941+58T>C	ENSP00000355759.5:n.1941+58T>C
NM_001618.3:c.1941+58T>C	NP_001609.2:n.1941+58T>C
NM_001618.4:c.1941+58T>C MANE Select	NP_001609.2:n.1941+58T>C