Canonical Allele Identifier: CA397851962

Gene: WRAP53

Linked Data

• MyVariant Identifiers: chr17:g.7606100T>G (hg19) ; chr17:g.7702782T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7702782T>G , CM000679.2:g.7702782T>G	GRCh38
NC_000017.10:g.7606100T>G , CM000679.1:g.7606100T>G	GRCh37
NC_000017.9:g.7546825T>G	NCBI36
NG_028245.1:g.21712T>G , LRG_375:g.21712T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000698742.1:c.1204T>G	ENSP00000513904.1:p.Tyr402Asp
ENST00000698743.1:c.*937T>G	ENSP00000513905.1:n.*937T>G
ENST00000698744.1:c.*864T>G	ENSP00000513906.1:n.*864T>G
ENST00000698745.1:c.*648T>G	ENSP00000513907.1:n.*648T>G
ENST00000698746.1:c.1204T>G	ENSP00000513908.1:p.Tyr402Asp
ENST00000698747.1:c.796T>G	ENSP00000513909.1:p.Tyr266Asp
ENST00000396463.7:c.1204T>G MANE Select	ENSP00000379727.3:p.Tyr402Asp
ENST00000316024.9:c.1204T>G	ENSP00000324203.5:p.Tyr402Asp
ENST00000396463.6:c.1204T>G	ENSP00000379727.2:p.Tyr402Asp
ENST00000431639.6:c.1204T>G	ENSP00000397219.2:p.Tyr402Asp
ENST00000457584.6:c.1204T>G	ENSP00000411061.2:p.Tyr402Asp
ENST00000463804.6:c.173T>G	ENSP00000465025.1:n.173T>G
ENST00000467699.5:n.2066T>G
ENST00000471973.6:n.475T>G
ENST00000498311.5:c.*372T>G	ENSP00000432991.1:n.*372T>G
ENST00000534050.5:c.1105T>G	ENSP00000434999.1:p.Tyr369Asp
NM_001143990.1:c.1204T>G	NP_001137462.1:p.Tyr402Asp
NM_001143991.1:c.1204T>G	NP_001137463.1:p.Tyr402Asp
NM_001143992.1:c.1204T>G	NP_001137464.1:p.Tyr402Asp
NM_018081.2:c.1204T>G , LRG_375t1:c.1204T>G	NP_060551.2:p.Tyr402Asp
XM_011523952.1:c.565T>G	XP_011522254.1:p.Tyr189Asp
XM_011523952.2:c.565T>G	XP_011522254.1:p.Tyr189Asp
XM_024450824.1:c.412T>G	XP_024306592.1:p.Tyr138Asp
XR_001752551.2:n.1481T>G
NM_001143991.2:c.1204T>G	NP_001137463.1:p.Tyr402Asp
NM_001143992.2:c.1204T>G MANE Select	NP_001137464.1:p.Tyr402Asp
NM_001143990.2:c.1204T>G	NP_001137462.1:p.Tyr402Asp