Canonical Allele Identifier: CA10703780

Gene: PARP1

Linked Data

• dbSNP Id: rs3219119
• gnomAD v2: 1-226556443-A-T
• gnomAD v3: 1-226368742-A-T
• gnomAD v4: 1-226368742-A-T
• MyVariant Identifiers: chr1:g.226556443A>T (hg19) ; chr1:g.226368742A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.226368742A>T , CM000663.2:g.226368742A>T	GRCh38
NC_000001.10:g.226556443A>T , CM000663.1:g.226556443A>T	GRCh37
NC_000001.9:g.224623066A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000366794.10:c.2155-421T>A MANE Select	ENSP00000355759.5:n.2155-421T>A
ENST00000498787.2:n.2314-421T>A
ENST00000676565.1:n.1927-421T>A
ENST00000676685.1:n.2380-421T>A
ENST00000676709.1:n.2380-421T>A
ENST00000677091.1:c.*837-421T>A	ENSP00000504745.1:n.*837-421T>A
ENST00000677189.1:n.208-421T>A
ENST00000677203.1:c.2026-421T>A	ENSP00000503396.1:n.2026-421T>A
ENST00000677374.1:n.3341-421T>A
ENST00000677884.1:n.2967-421T>A
ENST00000677985.1:n.145-421T>A
ENST00000678144.1:c.*975-421T>A	ENSP00000504430.1:n.*975-421T>A
ENST00000678226.1:n.1134-421T>A
ENST00000678288.1:n.280-421T>A
ENST00000678560.1:c.*2143-421T>A	ENSP00000503293.1:n.*2143-421T>A
ENST00000678781.1:n.2380-421T>A
ENST00000679276.1:n.2380-421T>A
ENST00000366794.9:c.2155-421T>A	ENSP00000355759.5:n.2155-421T>A
ENST00000490921.5:n.683-421T>A
ENST00000498787.1:n.211-421T>A
NM_001618.3:c.2155-421T>A	NP_001609.2:n.2155-421T>A
NM_001618.4:c.2155-421T>A MANE Select	NP_001609.2:n.2155-421T>A