Canonical Allele Identifier: CA2590178527
Gene: WRAP53 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7689064_7689080del , CM000679.2:g.7689064_7689080del GRCh38
NC_000017.10:g.7592382_7592398del , CM000679.1:g.7592382_7592398del GRCh37
NC_000017.9:g.7533107_7533123del NCBI36
NG_017013.2:g.3472_3488del , LRG_321:g.3472_3488del
NG_028245.1:g.7994_8010del , LRG_375:g.7994_8010del

Transcript Alleles

HGVS Amino-acid Change
ENST00000698742.1:c.416_431+1del
ENST00000698743.1:c.416_431+1del
ENST00000698744.1:c.416_431+1del
ENST00000698745.1:c.416_431+1del
ENST00000698746.1:c.416_431+1del
ENST00000396463.7:c.416_431+1del
ENST00000316024.9:c.416_431+1del
ENST00000396463.6:c.416_431+1del
ENST00000431639.6:c.416_431+1del
ENST00000457584.6:c.416_431+1del
ENST00000467699.5:n.502_517+1del
ENST00000498311.5:c.416_431+1del
ENST00000534050.5:c.416_431+1del
NM_001143990.1:c.416_431+1del
NM_001143991.1:c.416_431+1del
NM_001143992.1:c.416_431+1del
NM_018081.2:c.416_431+1del , LRG_375t1:c.416_431+1del
XM_011523952.2:c.-217_-202+1del
XM_024450824.1:c.-1660_-1645+1del
XM_024450825.1:c.416_431+1del
XR_001752551.2:n.661_676+1del
NM_001143991.2:c.416_431+1del
NM_001143992.2:c.416_431+1del
NM_001143990.2:c.416_431+1del