Canonical Allele Identifier: CA8354936
Gene: WRAP53 HGNC NCBI

Linked Data

dbSNP Id: rs751932334
gnomAD v2: 17-7592303-C-G
gnomAD v4: 17-7688985-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7688985C>G , CM000679.2:g.7688985C>G GRCh38
NC_000017.10:g.7592303C>G , CM000679.1:g.7592303C>G GRCh37
NC_000017.9:g.7533028C>G NCBI36
NG_017013.2:g.3566G>C , LRG_321:g.3566G>C
NG_028245.1:g.7915C>G , LRG_375:g.7915C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000698742.1:c.337C>G ENSP00000513904.1:p.Leu113Val
ENST00000698743.1:c.337C>G ENSP00000513905.1:p.Leu113Val
ENST00000698744.1:c.337C>G ENSP00000513906.1:p.Leu113Val
ENST00000698745.1:c.337C>G ENSP00000513907.1:p.Leu113Val
ENST00000698746.1:c.337C>G ENSP00000513908.1:p.Leu113Val
ENST00000396463.7:c.337C>G MANE Select ENSP00000379727.3:p.Leu113Val
ENST00000316024.9:c.337C>G ENSP00000324203.5:p.Leu113Val
ENST00000396463.6:c.337C>G ENSP00000379727.2:p.Leu113Val
ENST00000431639.6:c.337C>G ENSP00000397219.2:p.Leu113Val
ENST00000457584.6:c.337C>G ENSP00000411061.2:p.Leu113Val
ENST00000467699.5:n.423C>G
ENST00000498311.5:c.337C>G ENSP00000432991.1:p.Leu113Val
ENST00000534050.5:c.337C>G ENSP00000434999.1:p.Leu113Val
NM_001143990.1:c.337C>G NP_001137462.1:p.Leu113Val
NM_001143991.1:c.337C>G NP_001137463.1:p.Leu113Val
NM_001143992.1:c.337C>G NP_001137464.1:p.Leu113Val
NM_018081.2:c.337C>G , LRG_375t1:c.337C>G NP_060551.2:p.Leu113Val
XM_011523952.2:c.-296C>G XP_011522254.1:n.-296C>G
XM_024450824.1:c.-1739C>G XP_024306592.1:n.-1739C>G
XM_024450825.1:c.337C>G XP_024306593.1:p.Leu113Val
XR_001752551.2:n.582C>G
NM_001143991.2:c.337C>G NP_001137463.1:p.Leu113Val
NM_001143992.2:c.337C>G MANE Select NP_001137464.1:p.Leu113Val
NM_001143990.2:c.337C>G NP_001137462.1:p.Leu113Val