Canonical Allele Identifier: CA624706978

Gene: WRAP53

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7702330C>T , CM000679.2:g.7702330C>T	GRCh38
NC_000017.10:g.7605648C>T , CM000679.1:g.7605648C>T	GRCh37
NC_000017.9:g.7546373C>T	NCBI36
NG_028245.1:g.21260C>T , LRG_375:g.21260C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001143992.2:c.956-14C>T MANE Select	NP_001137464.1:n.956-14C>T
ENST00000396463.7:c.956-14C>T MANE Select	ENSP00000379727.3:n.956-14C>T
NM_001143990.1:c.956-14C>T	NP_001137462.1:n.956-14C>T
NM_001143990.2:c.956-14C>T	NP_001137462.1:n.956-14C>T
NM_001143991.1:c.956-14C>T	NP_001137463.1:n.956-14C>T
NM_001143991.2:c.956-14C>T	NP_001137463.1:n.956-14C>T
NM_001143992.1:c.956-14C>T	NP_001137464.1:n.956-14C>T
NM_018081.2:c.956-14C>T , LRG_375t1:c.956-14C>T	NP_060551.2:n.956-14C>T
ENST00000316024.9:c.956-14C>T	ENSP00000324203.5:n.956-14C>T
ENST00000396463.6:c.956-14C>T	ENSP00000379727.2:n.956-14C>T
ENST00000431639.6:c.956-14C>T	ENSP00000397219.2:n.956-14C>T
ENST00000457584.6:c.956-14C>T	ENSP00000411061.2:n.956-14C>T
ENST00000463804.6:c.134-413C>T	ENSP00000465025.1:n.134-413C>T
ENST00000467699.5:n.1614C>T
ENST00000471973.6:n.213C>T
ENST00000498311.5:c.*124-14C>T	ENSP00000432991.1:n.*124-14C>T
ENST00000534050.5:c.857-14C>T	ENSP00000434999.1:n.857-14C>T
ENST00000698742.1:c.956-14C>T	ENSP00000513904.1:n.956-14C>T
ENST00000698743.1:c.*689-14C>T	ENSP00000513905.1:n.*689-14C>T
ENST00000698744.1:c.*616-14C>T	ENSP00000513906.1:n.*616-14C>T
ENST00000698745.1:c.*400-14C>T	ENSP00000513907.1:n.*400-14C>T
ENST00000698746.1:c.956-14C>T	ENSP00000513908.1:n.956-14C>T
ENST00000698747.1:c.548-14C>T	ENSP00000513909.1:n.548-14C>T
XM_011523952.1:c.317-14C>T	XP_011522254.1:n.317-14C>T
XM_011523952.2:c.317-14C>T	XP_011522254.1:n.317-14C>T
XM_024450824.1:c.150C>T	XP_024306592.1:p.Phe50=
XR_001752551.2:n.1233-14C>T