Canonical Allele Identifier: CA2245954395

Gene: WRAP53

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7689177C= , CM000679.2:g.7689177C=	GRCh38
NC_000017.10:g.7592495C= , CM000679.1:g.7592495C=	GRCh37
NC_000017.9:g.7533220C=	NCBI36
NG_017013.2:g.3374G= , LRG_321:g.3374G=
NG_028245.1:g.8107C= , LRG_375:g.8107C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698742.1:c.432-47C=	ENSP00000513904.1:n.432-47C=
ENST00000698743.1:c.432-47C=	ENSP00000513905.1:n.432-47C=
ENST00000698744.1:c.432-47C=	ENSP00000513906.1:n.432-47C=
ENST00000698745.1:c.432-47C=	ENSP00000513907.1:n.432-47C=
ENST00000698746.1:c.432-47C=	ENSP00000513908.1:n.432-47C=
ENST00000396463.7:c.432-47C= MANE Select	ENSP00000379727.3:n.432-47C=
ENST00000316024.9:c.432-47C=	ENSP00000324203.5:n.432-47C=
ENST00000396463.6:c.432-47C=	ENSP00000379727.2:n.432-47C=
ENST00000431639.6:c.432-47C=	ENSP00000397219.2:n.432-47C=
ENST00000457584.6:c.432-47C=	ENSP00000411061.2:n.432-47C=
ENST00000467699.5:n.518-47C=
ENST00000498311.5:c.432-47C=	ENSP00000432991.1:n.432-47C=
ENST00000534050.5:c.431+98C=	ENSP00000434999.1:n.431+98C=
NM_001143990.1:c.432-47C=	NP_001137462.1:n.432-47C=
NM_001143991.1:c.432-47C=	NP_001137463.1:n.432-47C=
NM_001143992.1:c.432-47C=	NP_001137464.1:n.432-47C=
NM_018081.2:c.432-47C= , LRG_375t1:c.432-47C=	NP_060551.2:n.432-47C=
XM_011523952.2:c.-201-47C=	XP_011522254.1:n.-201-47C=
XM_024450824.1:c.-1644-47C=	XP_024306592.1:n.-1644-47C=
XM_024450825.1:c.432-47C=	XP_024306593.1:n.432-47C=
XR_001752551.2:n.677-47C=
NM_001143991.2:c.432-47C=	NP_001137463.1:n.432-47C=
NM_001143992.2:c.432-47C= MANE Select	NP_001137464.1:n.432-47C=
NM_001143990.2:c.432-47C=	NP_001137462.1:n.432-47C=