Canonical Allele Identifier: CA2245954405

Gene: WRAP53

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7689186_7689187delinsTG , CM000679.2:g.7689186_7689187delinsTG	GRCh38
NC_000017.10:g.7592504_7592505delinsTG , CM000679.1:g.7592504_7592505delinsTG	GRCh37
NC_000017.9:g.7533229_7533230delinsTG	NCBI36
NG_017013.2:g.3364_3365delinsCA , LRG_321:g.3364_3365delinsCA
NG_028245.1:g.8116_8117delinsTG , LRG_375:g.8116_8117delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698742.1:c.432-38_432-37delinsTG	ENSP00000513904.1:n.432-38_432-37delinsTG
ENST00000698743.1:c.432-38_432-37delinsTG	ENSP00000513905.1:n.432-38_432-37delinsTG
ENST00000698744.1:c.432-38_432-37delinsTG	ENSP00000513906.1:n.432-38_432-37delinsTG
ENST00000698745.1:c.432-38_432-37delinsTG	ENSP00000513907.1:n.432-38_432-37delinsTG
ENST00000698746.1:c.432-38_432-37delinsTG	ENSP00000513908.1:n.432-38_432-37delinsTG
ENST00000396463.7:c.432-38_432-37delinsTG MANE Select	ENSP00000379727.3:n.432-38_432-37delinsTG
ENST00000316024.9:c.432-38_432-37delinsTG	ENSP00000324203.5:n.432-38_432-37delinsTG
ENST00000396463.6:c.432-38_432-37delinsTG	ENSP00000379727.2:n.432-38_432-37delinsTG
ENST00000431639.6:c.432-38_432-37delinsTG	ENSP00000397219.2:n.432-38_432-37delinsTG
ENST00000457584.6:c.432-38_432-37delinsTG	ENSP00000411061.2:n.432-38_432-37delinsTG
ENST00000467699.5:n.518-38_518-37delinsTG
ENST00000498311.5:c.432-38_432-37delinsTG	ENSP00000432991.1:n.432-38_432-37delinsTG
ENST00000534050.5:c.431+107_431+108delinsTG	ENSP00000434999.1:n.431+107_431+108delinsTG
NM_001143990.1:c.432-38_432-37delinsTG	NP_001137462.1:n.432-38_432-37delinsTG
NM_001143991.1:c.432-38_432-37delinsTG	NP_001137463.1:n.432-38_432-37delinsTG
NM_001143992.1:c.432-38_432-37delinsTG	NP_001137464.1:n.432-38_432-37delinsTG
NM_018081.2:c.432-38_432-37delinsTG , LRG_375t1:c.432-38_432-37delinsTG	NP_060551.2:n.432-38_432-37delinsTG
XM_011523952.2:c.-201-38_-201-37delinsTG	XP_011522254.1:n.-201-38_-201-37delinsTG
XM_024450824.1:c.-1644-38_-1644-37delinsTG	XP_024306592.1:n.-1644-38_-1644-37delinsTG
XM_024450825.1:c.432-38_432-37delinsTG	XP_024306593.1:n.432-38_432-37delinsTG
XR_001752551.2:n.677-38_677-37delinsTG
NM_001143991.2:c.432-38_432-37delinsTG	NP_001137463.1:n.432-38_432-37delinsTG
NM_001143992.2:c.432-38_432-37delinsTG MANE Select	NP_001137464.1:n.432-38_432-37delinsTG
NM_001143990.2:c.432-38_432-37delinsTG	NP_001137462.1:n.432-38_432-37delinsTG