Canonical Allele Identifier: CA2245953327

Gene: WRAP53

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7688516C= , CM000679.2:g.7688516C=	GRCh38
NC_000017.10:g.7591834C= , CM000679.1:g.7591834C=	GRCh37
NC_000017.9:g.7532559C=	NCBI36
NG_017013.2:g.4035G= , LRG_321:g.4035G=
NG_028245.1:g.7446C= , LRG_375:g.7446C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698742.1:c.-47C=	ENSP00000513904.1:n.-47C=
ENST00000698743.1:c.-47C=	ENSP00000513905.1:n.-47C=
ENST00000698744.1:c.-47C=	ENSP00000513906.1:n.-47C=
ENST00000698745.1:c.-47C=	ENSP00000513907.1:n.-47C=
ENST00000698746.1:c.-47C=	ENSP00000513908.1:n.-47C=
ENST00000396463.7:c.-47C= MANE Select	ENSP00000379727.3:n.-47C=
ENST00000316024.9:c.-133C=	ENSP00000324203.5:n.-133C=
ENST00000396463.6:c.-47C=	ENSP00000379727.2:n.-47C=
ENST00000431639.6:c.-1-132C=	ENSP00000397219.2:n.-1-132C=
ENST00000457584.6:c.-1-132C=	ENSP00000411061.2:n.-1-132C=
ENST00000467699.5:n.40C=
ENST00000498311.5:c.-47C=	ENSP00000432991.1:n.-47C=
ENST00000534050.5:c.-133C=	ENSP00000434999.1:n.-133C=
NM_001143990.1:c.-1-132C=	NP_001137462.1:n.-1-132C=
NM_001143991.1:c.-1-132C=	NP_001137463.1:n.-1-132C=
NM_001143992.1:c.-47C=	NP_001137464.1:n.-47C=
NM_018081.2:c.-133C= , LRG_375t1:c.-133C=	NP_060551.2:n.-133C=
XM_024450824.1:c.-2122C=	XP_024306592.1:n.-2122C=
XM_024450825.1:c.-47C=	XP_024306593.1:n.-47C=
XR_001752551.2:n.199C=
NM_001143991.2:c.-1-132C=	NP_001137463.1:n.-1-132C=
NM_001143992.2:c.-47C= MANE Select	NP_001137464.1:n.-47C=
NM_001143990.2:c.-1-132C=	NP_001137462.1:n.-1-132C=