Canonical Allele Identifier: CA2245953194

Gene: WRAP53

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7688419T= , CM000679.2:g.7688419T=	GRCh38
NC_000017.10:g.7591737T= , CM000679.1:g.7591737T=	GRCh37
NC_000017.9:g.7532462T=	NCBI36
NG_017013.2:g.4132A= , LRG_321:g.4132A=
NG_028245.1:g.7349T= , LRG_375:g.7349T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698742.1:c.-144T=	ENSP00000513904.1:n.-144T=
ENST00000316024.9:c.-230T=	ENSP00000324203.5:n.-230T=
ENST00000396463.6:c.-144T=	ENSP00000379727.2:n.-144T=
ENST00000431639.6:c.-1-229T=	ENSP00000397219.2:n.-1-229T=
ENST00000457584.6:c.-1-229T=	ENSP00000411061.2:n.-1-229T=
ENST00000498311.5:c.-144T=	ENSP00000432991.1:n.-144T=
NM_001143990.1:c.-1-229T=	NP_001137462.1:n.-1-229T=
NM_001143991.1:c.-1-229T=	NP_001137463.1:n.-1-229T=
NM_001143992.1:c.-144T=	NP_001137464.1:n.-144T=
NM_018081.2:c.-230T= , LRG_375t1:c.-230T=	NP_060551.2:n.-230T=
XM_024450825.1:c.-144T=	XP_024306593.1:n.-144T=
XR_001752551.2:n.102T=
NM_001143991.2:c.-1-229T=	NP_001137463.1:n.-1-229T=
NM_001143990.2:c.-1-229T=	NP_001137462.1:n.-1-229T=