Canonical Allele Identifier: CA2245954342

Gene: WRAP53

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7689120G= , CM000679.2:g.7689120G=	GRCh38
NC_000017.10:g.7592438G= , CM000679.1:g.7592438G=	GRCh37
NC_000017.9:g.7533163G=	NCBI36
NG_017013.2:g.3431C= , LRG_321:g.3431C=
NG_028245.1:g.8050G= , LRG_375:g.8050G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698742.1:c.431+41G=	ENSP00000513904.1:n.431+41G=
ENST00000698743.1:c.431+41G=	ENSP00000513905.1:n.431+41G=
ENST00000698744.1:c.431+41G=	ENSP00000513906.1:n.431+41G=
ENST00000698745.1:c.431+41G=	ENSP00000513907.1:n.431+41G=
ENST00000698746.1:c.431+41G=	ENSP00000513908.1:n.431+41G=
ENST00000396463.7:c.431+41G= MANE Select	ENSP00000379727.3:n.431+41G=
ENST00000316024.9:c.431+41G=	ENSP00000324203.5:n.431+41G=
ENST00000396463.6:c.431+41G=	ENSP00000379727.2:n.431+41G=
ENST00000431639.6:c.431+41G=	ENSP00000397219.2:n.431+41G=
ENST00000457584.6:c.431+41G=	ENSP00000411061.2:n.431+41G=
ENST00000467699.5:n.517+41G=
ENST00000498311.5:c.431+41G=	ENSP00000432991.1:n.431+41G=
ENST00000534050.5:c.431+41G=	ENSP00000434999.1:n.431+41G=
NM_001143990.1:c.431+41G=	NP_001137462.1:n.431+41G=
NM_001143991.1:c.431+41G=	NP_001137463.1:n.431+41G=
NM_001143992.1:c.431+41G=	NP_001137464.1:n.431+41G=
NM_018081.2:c.431+41G= , LRG_375t1:c.431+41G=	NP_060551.2:n.431+41G=
XM_011523952.2:c.-202+41G=	XP_011522254.1:n.-202+41G=
XM_024450824.1:c.-1645+41G=	XP_024306592.1:n.-1645+41G=
XM_024450825.1:c.431+41G=	XP_024306593.1:n.431+41G=
XR_001752551.2:n.676+41G=
NM_001143991.2:c.431+41G=	NP_001137463.1:n.431+41G=
NM_001143992.2:c.431+41G= MANE Select	NP_001137464.1:n.431+41G=
NM_001143990.2:c.431+41G=	NP_001137462.1:n.431+41G=