Canonical Allele Identifier: CA8355388

Gene: WRAP53

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7703376C>G , CM000679.2:g.7703376C>G	GRCh38
NC_000017.10:g.7606694C>G , CM000679.1:g.7606694C>G	GRCh37
NC_000017.9:g.7547419C>G	NCBI36
NG_028245.1:g.22306C>G , LRG_375:g.22306C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001143992.2:c.1537C>G MANE Select	NP_001137464.1:p.Arg513Gly
ENST00000396463.7:c.1537C>G MANE Select	ENSP00000379727.3:p.Arg513Gly
NM_001143990.1:c.1537C>G	NP_001137462.1:p.Arg513Gly
NM_001143990.2:c.1537C>G	NP_001137462.1:p.Arg513Gly
NM_001143991.1:c.1537C>G	NP_001137463.1:p.Arg513Gly
NM_001143991.2:c.1537C>G	NP_001137463.1:p.Arg513Gly
NM_001143992.1:c.1537C>G	NP_001137464.1:p.Arg513Gly
NM_018081.2:c.1537C>G , LRG_375t1:c.1537C>G	NP_060551.2:p.Arg513Gly
ENST00000316024.9:c.1537C>G	ENSP00000324203.5:p.Arg513Gly
ENST00000396463.6:c.1537C>G	ENSP00000379727.2:p.Arg513Gly
ENST00000431639.6:c.1537C>G	ENSP00000397219.2:p.Arg513Gly
ENST00000457584.6:c.1537C>G	ENSP00000411061.2:p.Arg513Gly
ENST00000467699.5:n.2399C>G
ENST00000471973.6:n.872C>G
ENST00000498114.1:n.381C>G
ENST00000498311.5:c.*705C>G	ENSP00000432991.1:n.*705C>G
ENST00000534050.5:c.1438C>G	ENSP00000434999.1:p.Arg480Gly
ENST00000698743.1:c.*1270C>G	ENSP00000513905.1:n.*1270C>G
ENST00000698744.1:c.*1197C>G	ENSP00000513906.1:n.*1197C>G
ENST00000698745.1:c.*981C>G	ENSP00000513907.1:n.*981C>G
ENST00000698746.1:c.1402C>G	ENSP00000513908.1:p.Arg468Gly
ENST00000698747.1:c.1129C>G	ENSP00000513909.1:p.Arg377Gly
XM_011523952.1:c.898C>G	XP_011522254.1:p.Arg300Gly
XM_011523952.2:c.898C>G	XP_011522254.1:p.Arg300Gly
XM_024450824.1:c.745C>G	XP_024306592.1:p.Arg249Gly
XR_001752551.2:n.1814C>G