Canonical Allele Identifier: CA2245953314

Gene: WRAP53

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7688509G= , CM000679.2:g.7688509G=	GRCh38
NC_000017.10:g.7591827G= , CM000679.1:g.7591827G=	GRCh37
NC_000017.9:g.7532552G=	NCBI36
NG_017013.2:g.4042C= , LRG_321:g.4042C=
NG_028245.1:g.7439G= , LRG_375:g.7439G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698742.1:c.-54G=	ENSP00000513904.1:n.-54G=
ENST00000698743.1:c.-54G=	ENSP00000513905.1:n.-54G=
ENST00000698744.1:c.-54G=	ENSP00000513906.1:n.-54G=
ENST00000698745.1:c.-54G=	ENSP00000513907.1:n.-54G=
ENST00000698746.1:c.-54G=	ENSP00000513908.1:n.-54G=
ENST00000396463.7:c.-54G= MANE Select	ENSP00000379727.3:n.-54G=
ENST00000316024.9:c.-140G=	ENSP00000324203.5:n.-140G=
ENST00000396463.6:c.-54G=	ENSP00000379727.2:n.-54G=
ENST00000431639.6:c.-1-139G=	ENSP00000397219.2:n.-1-139G=
ENST00000457584.6:c.-1-139G=	ENSP00000411061.2:n.-1-139G=
ENST00000467699.5:n.33G=
ENST00000498311.5:c.-54G=	ENSP00000432991.1:n.-54G=
ENST00000534050.5:c.-140G=	ENSP00000434999.1:n.-140G=
NM_001143990.1:c.-1-139G=	NP_001137462.1:n.-1-139G=
NM_001143991.1:c.-1-139G=	NP_001137463.1:n.-1-139G=
NM_001143992.1:c.-54G=	NP_001137464.1:n.-54G=
NM_018081.2:c.-140G= , LRG_375t1:c.-140G=	NP_060551.2:n.-140G=
XM_024450824.1:c.-2129G=	XP_024306592.1:n.-2129G=
XM_024450825.1:c.-54G=	XP_024306593.1:n.-54G=
XR_001752551.2:n.192G=
NM_001143991.2:c.-1-139G=	NP_001137463.1:n.-1-139G=
NM_001143992.2:c.-54G= MANE Select	NP_001137464.1:n.-54G=
NM_001143990.2:c.-1-139G=	NP_001137462.1:n.-1-139G=