Canonical Allele Identifier: CA8354905
Gene: WRAP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 2816665
ClinVar RCV Id: RCV003720950
dbSNP Id: rs761413179
gnomAD v2: 17-7592164-G-A
gnomAD v4: 17-7688846-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7688846G>A , CM000679.2:g.7688846G>A GRCh38
NC_000017.10:g.7592164G>A , CM000679.1:g.7592164G>A GRCh37
NC_000017.9:g.7532889G>A NCBI36
NG_017013.2:g.3705C>T , LRG_321:g.3705C>T
NG_028245.1:g.7776G>A , LRG_375:g.7776G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000698742.1:c.198G>A ENSP00000513904.1:p.Glu66=
ENST00000698743.1:c.198G>A ENSP00000513905.1:p.Glu66=
ENST00000698744.1:c.198G>A ENSP00000513906.1:p.Glu66=
ENST00000698745.1:c.198G>A ENSP00000513907.1:p.Glu66=
ENST00000698746.1:c.198G>A ENSP00000513908.1:p.Glu66=
ENST00000396463.7:c.198G>A MANE Select ENSP00000379727.3:p.Glu66=
ENST00000316024.9:c.198G>A ENSP00000324203.5:p.Glu66=
ENST00000396463.6:c.198G>A ENSP00000379727.2:p.Glu66=
ENST00000431639.6:c.198G>A ENSP00000397219.2:p.Glu66=
ENST00000457584.6:c.198G>A ENSP00000411061.2:p.Glu66=
ENST00000467699.5:n.284G>A
ENST00000498311.5:c.198G>A ENSP00000432991.1:p.Glu66=
ENST00000534050.5:c.198G>A ENSP00000434999.1:p.Glu66=
NM_001143990.1:c.198G>A NP_001137462.1:p.Glu66=
NM_001143991.1:c.198G>A NP_001137463.1:p.Glu66=
NM_001143992.1:c.198G>A NP_001137464.1:p.Glu66=
NM_018081.2:c.198G>A , LRG_375t1:c.198G>A NP_060551.2:p.Glu66=
XM_011523952.2:c.-435G>A XP_011522254.1:n.-435G>A
XM_024450824.1:c.-1878G>A XP_024306592.1:n.-1878G>A
XM_024450825.1:c.198G>A XP_024306593.1:p.Glu66=
XR_001752551.2:n.443G>A
NM_001143991.2:c.198G>A NP_001137463.1:p.Glu66=
NM_001143992.2:c.198G>A MANE Select NP_001137464.1:p.Glu66=
NM_001143990.2:c.198G>A NP_001137462.1:p.Glu66=