Canonical Allele Identifier: CA2499224983
Gene: WRAP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 1169853
ClinVar RCV Id: RCV001521649
dbSNP Id: rs2151097825

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7703404_7703405delinsGA , CM000679.2:g.7703404_7703405delinsGA GRCh38
NC_000017.10:g.7606722_7606723delinsGA , CM000679.1:g.7606722_7606723delinsGA GRCh37
NC_000017.9:g.7547447_7547448delinsGA NCBI36
NG_028245.1:g.22334_22335delinsGA , LRG_375:g.22334_22335delinsGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000698743.1:c.*1298_*1299delinsGA ENSP00000513905.1:n.*1298_*1299delinsGA
ENST00000698744.1:c.*1225_*1226delinsGA ENSP00000513906.1:n.*1225_*1226delinsGA
ENST00000698745.1:c.*1009_*1010delinsGA ENSP00000513907.1:n.*1009_*1010delinsGA
ENST00000698746.1:c.1430_1431delinsGA ENSP00000513908.1:p.Ala477Gly
ENST00000698747.1:c.1157_1158delinsGA ENSP00000513909.1:p.Ala386Gly
ENST00000396463.7:c.1565_1566delinsGA MANE Select ENSP00000379727.3:p.Ala522Gly
ENST00000316024.9:c.1565_1566delinsGA ENSP00000324203.5:p.Ala522Gly
ENST00000396463.6:c.1565_1566delinsGA ENSP00000379727.2:p.Ala522Gly
ENST00000431639.6:c.1565_1566delinsGA ENSP00000397219.2:p.Ala522Gly
ENST00000457584.6:c.1565_1566delinsGA ENSP00000411061.2:p.Ala522Gly
ENST00000467699.5:n.2427_2428delinsGA
ENST00000471973.6:n.900_901delinsGA
ENST00000498114.1:n.409_410delinsGA
ENST00000498311.5:c.*733_*734delinsGA ENSP00000432991.1:n.*733_*734delinsGA
ENST00000534050.5:c.1466_1467delinsGA ENSP00000434999.1:p.Ala489Gly
NM_001143990.1:c.1565_1566delinsGA NP_001137462.1:p.Ala522Gly
NM_001143991.1:c.1565_1566delinsGA NP_001137463.1:p.Ala522Gly
NM_001143992.1:c.1565_1566delinsGA NP_001137464.1:p.Ala522Gly
NM_018081.2:c.1565_1566delinsGA , LRG_375t1:c.1565_1566delinsGA NP_060551.2:p.Ala522Gly
XM_011523952.1:c.926_927delinsGA XP_011522254.1:p.Ala309Gly
XM_011523952.2:c.926_927delinsGA XP_011522254.1:p.Ala309Gly
XM_024450824.1:c.773_774delinsGA XP_024306592.1:p.Ala258Gly
XR_001752551.2:n.1842_1843delinsGA
NM_001143991.2:c.1565_1566delinsGA NP_001137463.1:p.Ala522Gly
NM_001143992.2:c.1565_1566delinsGA MANE Select NP_001137464.1:p.Ala522Gly
NM_001143990.2:c.1565_1566delinsGA NP_001137462.1:p.Ala522Gly