Canonical Allele Identifier: CA397854264

Gene: WRAP53

Genomic Alleles

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

Transcript Alleles

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