Canonical Allele Identifier: CA344264

Gene: WRAP53

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7703027G>A , CM000679.2:g.7703027G>A	GRCh38
NC_000017.10:g.7606345G>A , CM000679.1:g.7606345G>A	GRCh37
NC_000017.9:g.7547070G>A	NCBI36
NG_028245.1:g.21957G>A , LRG_375:g.21957G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001143992.2:c.1303G>A MANE Select	NP_001137464.1:p.Gly435Arg
ENST00000396463.7:c.1303G>A MANE Select	ENSP00000379727.3:p.Gly435Arg
NM_001143990.1:c.1303G>A	NP_001137462.1:p.Gly435Arg
NM_001143990.2:c.1303G>A	NP_001137462.1:p.Gly435Arg
NM_001143991.1:c.1303G>A	NP_001137463.1:p.Gly435Arg
NM_001143991.2:c.1303G>A	NP_001137463.1:p.Gly435Arg
NM_001143992.1:c.1303G>A	NP_001137464.1:p.Gly435Arg
NM_018081.2:c.1303G>A , LRG_375t1:c.1303G>A	NP_060551.2:p.Gly435Arg
ENST00000316024.9:c.1303G>A	ENSP00000324203.5:p.Gly435Arg
ENST00000396463.6:c.1303G>A	ENSP00000379727.2:p.Gly435Arg
ENST00000431639.6:c.1303G>A	ENSP00000397219.2:p.Gly435Arg
ENST00000457584.6:c.1303G>A	ENSP00000411061.2:p.Gly435Arg
ENST00000463804.6:c.272G>A	ENSP00000465025.1:n.272G>A
ENST00000467699.5:n.2165G>A
ENST00000471973.6:n.638G>A
ENST00000498114.1:n.147G>A
ENST00000498311.5:c.*471G>A	ENSP00000432991.1:n.*471G>A
ENST00000534050.5:c.1204G>A	ENSP00000434999.1:p.Gly402Arg
ENST00000698742.1:c.1303G>A	ENSP00000513904.1:p.Gly435Arg
ENST00000698743.1:c.*1036G>A	ENSP00000513905.1:n.*1036G>A
ENST00000698744.1:c.*963G>A	ENSP00000513906.1:n.*963G>A
ENST00000698745.1:c.*747G>A	ENSP00000513907.1:n.*747G>A
ENST00000698746.1:c.1268+181G>A	ENSP00000513908.1:n.1268+181G>A
ENST00000698747.1:c.895G>A	ENSP00000513909.1:p.Gly299Arg
XM_011523952.1:c.664G>A	XP_011522254.1:p.Gly222Arg
XM_011523952.2:c.664G>A	XP_011522254.1:p.Gly222Arg
XM_024450824.1:c.511G>A	XP_024306592.1:p.Gly171Arg
XR_001752551.2:n.1580G>A