Canonical Allele Identifier: CA397858897

Gene: WRAP53

Linked Data

• MyVariant Identifiers: chr17:g.7592316A>T (hg19) ; chr17:g.7688998A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7688998A>T , CM000679.2:g.7688998A>T	GRCh38
NC_000017.10:g.7592316A>T , CM000679.1:g.7592316A>T	GRCh37
NC_000017.9:g.7533041A>T	NCBI36
NG_017013.2:g.3553T>A , LRG_321:g.3553T>A
NG_028245.1:g.7928A>T , LRG_375:g.7928A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698742.1:c.350A>T	ENSP00000513904.1:p.Glu117Val
ENST00000698743.1:c.350A>T	ENSP00000513905.1:p.Glu117Val
ENST00000698744.1:c.350A>T	ENSP00000513906.1:p.Glu117Val
ENST00000698745.1:c.350A>T	ENSP00000513907.1:p.Glu117Val
ENST00000698746.1:c.350A>T	ENSP00000513908.1:p.Glu117Val
ENST00000396463.7:c.350A>T MANE Select	ENSP00000379727.3:p.Glu117Val
ENST00000316024.9:c.350A>T	ENSP00000324203.5:p.Glu117Val
ENST00000396463.6:c.350A>T	ENSP00000379727.2:p.Glu117Val
ENST00000431639.6:c.350A>T	ENSP00000397219.2:p.Glu117Val
ENST00000457584.6:c.350A>T	ENSP00000411061.2:p.Glu117Val
ENST00000467699.5:n.436A>T
ENST00000498311.5:c.350A>T	ENSP00000432991.1:p.Glu117Val
ENST00000534050.5:c.350A>T	ENSP00000434999.1:p.Glu117Val
NM_001143990.1:c.350A>T	NP_001137462.1:p.Glu117Val
NM_001143991.1:c.350A>T	NP_001137463.1:p.Glu117Val
NM_001143992.1:c.350A>T	NP_001137464.1:p.Glu117Val
NM_018081.2:c.350A>T , LRG_375t1:c.350A>T	NP_060551.2:p.Glu117Val
XM_011523952.2:c.-283A>T	XP_011522254.1:n.-283A>T
XM_024450824.1:c.-1726A>T	XP_024306592.1:n.-1726A>T
XM_024450825.1:c.350A>T	XP_024306593.1:p.Glu117Val
XR_001752551.2:n.595A>T
NM_001143991.2:c.350A>T	NP_001137463.1:p.Glu117Val
NM_001143992.2:c.350A>T MANE Select	NP_001137464.1:p.Glu117Val
NM_001143990.2:c.350A>T	NP_001137462.1:p.Glu117Val