Canonical Allele Identifier: CA2245953267

Gene: WRAP53

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7688479T= , CM000679.2:g.7688479T=	GRCh38
NC_000017.10:g.7591797T= , CM000679.1:g.7591797T=	GRCh37
NC_000017.9:g.7532522T=	NCBI36
NG_017013.2:g.4072A= , LRG_321:g.4072A=
NG_028245.1:g.7409T= , LRG_375:g.7409T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698742.1:c.-84T=	ENSP00000513904.1:n.-84T=
ENST00000698743.1:c.-84T=	ENSP00000513905.1:n.-84T=
ENST00000698744.1:c.-84T=	ENSP00000513906.1:n.-84T=
ENST00000698745.1:c.-84T=	ENSP00000513907.1:n.-84T=
ENST00000698746.1:c.-84T=	ENSP00000513908.1:n.-84T=
ENST00000396463.7:c.-84T= MANE Select	ENSP00000379727.3:n.-84T=
ENST00000316024.9:c.-170T=	ENSP00000324203.5:n.-170T=
ENST00000396463.6:c.-84T=	ENSP00000379727.2:n.-84T=
ENST00000431639.6:c.-1-169T=	ENSP00000397219.2:n.-1-169T=
ENST00000457584.6:c.-1-169T=	ENSP00000411061.2:n.-1-169T=
ENST00000467699.5:n.3T=
ENST00000498311.5:c.-84T=	ENSP00000432991.1:n.-84T=
ENST00000534050.5:c.-170T=	ENSP00000434999.1:n.-170T=
NM_001143990.1:c.-1-169T=	NP_001137462.1:n.-1-169T=
NM_001143991.1:c.-1-169T=	NP_001137463.1:n.-1-169T=
NM_001143992.1:c.-84T=	NP_001137464.1:n.-84T=
NM_018081.2:c.-170T= , LRG_375t1:c.-170T=	NP_060551.2:n.-170T=
XM_024450824.1:c.-2159T=	XP_024306592.1:n.-2159T=
XM_024450825.1:c.-84T=	XP_024306593.1:n.-84T=
XR_001752551.2:n.162T=
NM_001143991.2:c.-1-169T=	NP_001137463.1:n.-1-169T=
NM_001143992.2:c.-84T= MANE Select	NP_001137464.1:n.-84T=
NM_001143990.2:c.-1-169T=	NP_001137462.1:n.-1-169T=