Canonical Allele Identifier: CA10754097
Gene: PARP1 HGNC NCBI

Linked Data

dbSNP Id: rs1805410

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.226380964T>C , CM000663.2:g.226380964T>C GRCh38
NC_000001.10:g.226568665T>C , CM000663.1:g.226568665T>C GRCh37
NC_000001.9:g.224635288T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000366794.10:c.1300+104A>G MANE Select ENSP00000355759.5:n.1300+104A>G
ENST00000676685.1:n.1525+104A>G
ENST00000676709.1:n.1525+104A>G
ENST00000677091.1:c.1093-800A>G ENSP00000504745.1:n.1093-800A>G
ENST00000677203.1:c.1300+104A>G ENSP00000503396.1:n.1300+104A>G
ENST00000677374.1:n.1687A>G
ENST00000677884.1:n.2112+104A>G
ENST00000678144.1:c.*120+104A>G ENSP00000504430.1:n.*120+104A>G
ENST00000678226.1:n.279+104A>G
ENST00000678560.1:c.*1288+104A>G ENSP00000503293.1:n.*1288+104A>G
ENST00000678781.1:n.1525+104A>G
ENST00000679276.1:n.1525+104A>G
ENST00000366794.9:c.1300+104A>G ENSP00000355759.5:n.1300+104A>G
NM_001618.3:c.1300+104A>G NP_001609.2:n.1300+104A>G
NM_001618.4:c.1300+104A>G MANE Select NP_001609.2:n.1300+104A>G