Canonical Allele Identifier: CA354165906
Gene: PARP9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.122528439A>C , CM000665.2:g.122528439A>C GRCh38
NC_000003.11:g.122247286A>C , CM000665.1:g.122247286A>C GRCh37
NC_000003.10:g.123729976A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000682323.1:c.2385T>G MANE Select ENSP00000507390.1:p.Asp795Glu
ENST00000360356.6:c.2490T>G ENSP00000353512.2:p.Asp830Glu
ENST00000471785.5:c.2385T>G ENSP00000419001.1:p.Asp795Glu
ENST00000477522.6:c.2385T>G ENSP00000419506.1:p.Asp795Glu
ENST00000489652.1:n.2164T>G
ENST00000492382.5:c.1125T>G ENSP00000417664.1:p.Asp375Glu
NM_001146102.1:c.2490T>G NP_001139574.1:p.Asp830Glu
NM_001146103.1:c.2385T>G NP_001139575.1:p.Asp795Glu
NM_001146104.1:c.2385T>G NP_001139576.1:p.Asp795Glu
NM_001146105.1:c.2385T>G NP_001139577.1:p.Asp795Glu
NM_031458.2:c.2490T>G NP_113646.2:p.Asp830Glu
XM_005247820.1:c.2490T>G XP_005247877.1:p.Asp830Glu
XR_924404.1:n.345+648A>C
XR_924405.1:n.514+648A>C
XR_924406.1:n.369+648A>C
XM_005247820.2:c.2490T>G XP_005247877.1:p.Asp830Glu
XM_017007304.1:c.2490T>G XP_016862793.1:p.Asp830Glu
XM_017007305.2:c.2385T>G XP_016862794.1:p.Asp795Glu
XM_017007306.1:c.2385T>G XP_016862795.1:p.Asp795Glu
XR_001740305.1:n.2729T>G
XR_001740306.2:n.2627T>G
XR_001740869.1:n.579+648A>C
XR_002959597.1:n.2870T>G
XR_924405.3:n.579+648A>C
NM_001146102.2:c.2490T>G NP_001139574.1:p.Asp830Glu
NM_001146103.2:c.2385T>G NP_001139575.1:p.Asp795Glu
NM_001146104.2:c.2385T>G NP_001139576.1:p.Asp795Glu
NM_001146105.2:c.2385T>G MANE Select NP_001139577.1:p.Asp795Glu
NM_031458.3:c.2490T>G NP_113646.2:p.Asp830Glu
NM_001387871.1:c.2490T>G NP_001374800.1:p.Asp830Glu
NM_001387872.1:c.2490T>G NP_001374801.1:p.Asp830Glu
NM_001387873.1:c.2424T>G NP_001374802.1:p.Asp808Glu
NM_001387874.1:c.2424T>G NP_001374803.1:p.Asp808Glu
NM_001387875.1:c.2385T>G NP_001374804.1:p.Asp795Glu
NM_001387876.1:c.2385T>G NP_001374805.1:p.Asp795Glu
NM_001387877.1:c.2385T>G NP_001374806.1:p.Asp795Glu
NM_001387878.1:c.*324T>G NP_001374807.1:n.*324T>G
NM_001387879.1:c.*324T>G NP_001374808.1:n.*324T>G
NM_001387881.1:c.*324T>G NP_001374810.1:n.*324T>G
NM_001387882.1:c.*324T>G NP_001374811.1:n.*324T>G
NM_001387883.1:c.*324T>G NP_001374812.1:n.*324T>G
NM_001387884.1:c.*324T>G NP_001374813.1:n.*324T>G
NR_170857.1:n.3699T>G
NR_170858.1:n.3821T>G
NR_170859.1:n.3406T>G
NR_170860.1:n.3531T>G
NR_170861.1:n.3511T>G
NR_170862.1:n.3409T>G
NR_170864.1:n.2652T>G
NR_170865.1:n.2786T>G