Canonical Allele Identifier: CA2245954368
Gene: WRAP53 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7689150_7689158delinsTGAGACCCA , CM000679.2:g.7689150_7689158delinsTGAGACCCA GRCh38
NC_000017.10:g.7592468_7592476delinsTGAGACCCA , CM000679.1:g.7592468_7592476delinsTGAGACCCA GRCh37
NC_000017.9:g.7533193_7533201delinsTGAGACCCA NCBI36
NG_017013.2:g.3393_3401delinsTGGGTCTCA , LRG_321:g.3393_3401delinsTGGGTCTCA
NG_028245.1:g.8080_8088delinsTGAGACCCA , LRG_375:g.8080_8088delinsTGAGACCCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000698742.1:c.431+71_432-66delinsTGAGACCCA ENSP00000513904.1:n.431+71_432-66delinsTGAGACCCA
ENST00000698743.1:c.431+71_432-66delinsTGAGACCCA ENSP00000513905.1:n.431+71_432-66delinsTGAGACCCA
ENST00000698744.1:c.431+71_432-66delinsTGAGACCCA ENSP00000513906.1:n.431+71_432-66delinsTGAGACCCA
ENST00000698745.1:c.431+71_432-66delinsTGAGACCCA ENSP00000513907.1:n.431+71_432-66delinsTGAGACCCA
ENST00000698746.1:c.431+71_432-66delinsTGAGACCCA ENSP00000513908.1:n.431+71_432-66delinsTGAGACCCA
ENST00000396463.7:c.431+71_432-66delinsTGAGACCCA MANE Select ENSP00000379727.3:n.431+71_432-66delinsTGAGACCCA
ENST00000316024.9:c.431+71_432-66delinsTGAGACCCA ENSP00000324203.5:n.431+71_432-66delinsTGAGACCCA
ENST00000396463.6:c.431+71_432-66delinsTGAGACCCA ENSP00000379727.2:n.431+71_432-66delinsTGAGACCCA
ENST00000431639.6:c.431+71_432-66delinsTGAGACCCA ENSP00000397219.2:n.431+71_432-66delinsTGAGACCCA
ENST00000457584.6:c.431+71_432-66delinsTGAGACCCA ENSP00000411061.2:n.431+71_432-66delinsTGAGACCCA
ENST00000467699.5:n.517+71_518-66delinsTGAGACCCA
ENST00000498311.5:c.431+71_432-66delinsTGAGACCCA ENSP00000432991.1:n.431+71_432-66delinsTGAGACCCA
ENST00000534050.5:c.431+71_431+79delinsTGAGACCCA ENSP00000434999.1:n.431+71_431+79delinsTGAGACCCA
NM_001143990.1:c.431+71_432-66delinsTGAGACCCA NP_001137462.1:n.431+71_432-66delinsTGAGACCCA
NM_001143991.1:c.431+71_432-66delinsTGAGACCCA NP_001137463.1:n.431+71_432-66delinsTGAGACCCA
NM_001143992.1:c.431+71_432-66delinsTGAGACCCA NP_001137464.1:n.431+71_432-66delinsTGAGACCCA
NM_018081.2:c.431+71_432-66delinsTGAGACCCA , LRG_375t1:c.431+71_432-66delinsTGAGACCCA NP_060551.2:n.431+71_432-66delinsTGAGACCCA
XM_011523952.2:c.-202+71_-201-66delinsTGAGACCCA XP_011522254.1:n.-202+71_-201-66delinsTGAGACCCA
XM_024450824.1:c.-1645+71_-1644-66delinsTGAGACCCA XP_024306592.1:n.-1645+71_-1644-66delinsTGAGACCCA
XM_024450825.1:c.431+71_432-66delinsTGAGACCCA XP_024306593.1:n.431+71_432-66delinsTGAGACCCA
XR_001752551.2:n.676+71_677-66delinsTGAGACCCA
NM_001143991.2:c.431+71_432-66delinsTGAGACCCA NP_001137463.1:n.431+71_432-66delinsTGAGACCCA
NM_001143992.2:c.431+71_432-66delinsTGAGACCCA MANE Select NP_001137464.1:n.431+71_432-66delinsTGAGACCCA
NM_001143990.2:c.431+71_432-66delinsTGAGACCCA NP_001137462.1:n.431+71_432-66delinsTGAGACCCA