Canonical Allele Identifier: CA497926980

Gene: WRAP53

Linked Data

• dbSNP Id: rs1160488955
• gnomAD v2: 17-7606093-G-A
• gnomAD v4: 17-7702775-G-A
• MyVariant Identifiers: chr17:g.7606093G>A (hg19) ; chr17:g.7702775G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7702775G>A , CM000679.2:g.7702775G>A	GRCh38
NC_000017.10:g.7606093G>A , CM000679.1:g.7606093G>A	GRCh37
NC_000017.9:g.7546818G>A	NCBI36
NG_028245.1:g.21705G>A , LRG_375:g.21705G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000698742.1:c.1197G>A	ENSP00000513904.1:p.Gln399=
ENST00000698743.1:c.*930G>A	ENSP00000513905.1:n.*930G>A
ENST00000698744.1:c.*857G>A	ENSP00000513906.1:n.*857G>A
ENST00000698745.1:c.*641G>A	ENSP00000513907.1:n.*641G>A
ENST00000698746.1:c.1197G>A	ENSP00000513908.1:p.Gln399=
ENST00000698747.1:c.789G>A	ENSP00000513909.1:p.Gln263=
ENST00000396463.7:c.1197G>A MANE Select	ENSP00000379727.3:p.Gln399=
ENST00000316024.9:c.1197G>A	ENSP00000324203.5:p.Gln399=
ENST00000396463.6:c.1197G>A	ENSP00000379727.2:p.Gln399=
ENST00000431639.6:c.1197G>A	ENSP00000397219.2:p.Gln399=
ENST00000457584.6:c.1197G>A	ENSP00000411061.2:p.Gln399=
ENST00000463804.6:c.166G>A	ENSP00000465025.1:n.166G>A
ENST00000467699.5:n.2059G>A
ENST00000471973.6:n.468G>A
ENST00000498311.5:c.*365G>A	ENSP00000432991.1:n.*365G>A
ENST00000534050.5:c.1098G>A	ENSP00000434999.1:p.Gln366=
NM_001143990.1:c.1197G>A	NP_001137462.1:p.Gln399=
NM_001143991.1:c.1197G>A	NP_001137463.1:p.Gln399=
NM_001143992.1:c.1197G>A	NP_001137464.1:p.Gln399=
NM_018081.2:c.1197G>A , LRG_375t1:c.1197G>A	NP_060551.2:p.Gln399=
XM_011523952.1:c.558G>A	XP_011522254.1:p.Gln186=
XM_011523952.2:c.558G>A	XP_011522254.1:p.Gln186=
XM_024450824.1:c.405G>A	XP_024306592.1:p.Gln135=
XR_001752551.2:n.1474G>A
NM_001143991.2:c.1197G>A	NP_001137463.1:p.Gln399=
NM_001143992.2:c.1197G>A MANE Select	NP_001137464.1:p.Gln399=
NM_001143990.2:c.1197G>A	NP_001137462.1:p.Gln399=