Canonical Allele Identifier: CA383658193

Gene: PARP11

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.3814142C>G , CM000674.2:g.3814142C>G	GRCh38
NC_000012.11:g.3923308C>G , CM000674.1:g.3923308C>G	GRCh37
NC_000012.10:g.3793569C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_020367.6:c.595G>C MANE Select	NP_065100.2:p.Glu199Gln
ENST00000228820.9:c.595G>C MANE Select	ENSP00000228820.4:p.Glu199Gln
NM_001286521.1:c.352G>C	NP_001273450.1:p.Glu118Gln
NM_001286521.2:c.352G>C	NP_001273450.1:p.Glu118Gln
NM_001286522.1:c.352G>C	NP_001273451.1:p.Glu118Gln
NM_001286522.2:c.352G>C	NP_001273451.1:p.Glu118Gln
NM_020367.5:c.595G>C	NP_065100.2:p.Glu199Gln
NR_104461.1:n.873G>C
NR_104461.2:n.824G>C
ENST00000228820.8:c.595G>C	ENSP00000228820.4:p.Glu199Gln
ENST00000416739.5:c.595G>C	ENSP00000392392.1:p.Glu199Gln
ENST00000427057.6:c.352G>C	ENSP00000397058.2:p.Glu118Gln
ENST00000447133.7:c.352G>C	ENSP00000405385.3:p.Glu118Gln
ENST00000453942.2:c.*96G>C	ENSP00000395062.2:n.*96G>C
ENST00000458162.6:c.*321G>C	ENSP00000399665.2:n.*321G>C
ENST00000476985.5:n.149G>C
XM_005253711.3:c.574G>C	XP_005253768.1:p.Glu192Gln
XM_005253714.3:c.298G>C	XP_005253771.1:p.Glu100Gln
XM_011520970.1:c.574G>C	XP_011519272.1:p.Glu192Gln
XM_011520970.2:c.574G>C	XP_011519272.1:p.Glu192Gln
XM_011520971.1:c.574G>C	XP_011519273.1:p.Glu192Gln
XM_011520973.1:c.574G>C	XP_011519275.1:p.Glu192Gln
XM_011520973.2:c.574G>C	XP_011519275.1:p.Glu192Gln
XM_017019671.1:c.352G>C	XP_016875160.1:p.Glu118Gln