Canonical Allele Identifier: CA397851872

Gene: WRAP53

Linked Data

• dbSNP Id: rs768411006
• gnomAD v3: 17-7702771-G-C
• gnomAD v4: 17-7702771-G-C
• MyVariant Identifiers: chr17:g.7606089G>C (hg19) ; chr17:g.7702771G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7702771G>C , CM000679.2:g.7702771G>C	GRCh38
NC_000017.10:g.7606089G>C , CM000679.1:g.7606089G>C	GRCh37
NC_000017.9:g.7546814G>C	NCBI36
NG_028245.1:g.21701G>C , LRG_375:g.21701G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000698742.1:c.1193G>C	ENSP00000513904.1:p.Arg398Pro
ENST00000698743.1:c.*926G>C	ENSP00000513905.1:n.*926G>C
ENST00000698744.1:c.*853G>C	ENSP00000513906.1:n.*853G>C
ENST00000698745.1:c.*637G>C	ENSP00000513907.1:n.*637G>C
ENST00000698746.1:c.1193G>C	ENSP00000513908.1:p.Arg398Pro
ENST00000698747.1:c.785G>C	ENSP00000513909.1:p.Arg262Pro
ENST00000396463.7:c.1193G>C MANE Select	ENSP00000379727.3:p.Arg398Pro
ENST00000316024.9:c.1193G>C	ENSP00000324203.5:p.Arg398Pro
ENST00000396463.6:c.1193G>C	ENSP00000379727.2:p.Arg398Pro
ENST00000431639.6:c.1193G>C	ENSP00000397219.2:p.Arg398Pro
ENST00000457584.6:c.1193G>C	ENSP00000411061.2:p.Arg398Pro
ENST00000463804.6:c.162G>C	ENSP00000465025.1:n.162G>C
ENST00000467699.5:n.2055G>C
ENST00000471973.6:n.464G>C
ENST00000498311.5:c.*361G>C	ENSP00000432991.1:n.*361G>C
ENST00000534050.5:c.1094G>C	ENSP00000434999.1:p.Arg365Pro
NM_001143990.1:c.1193G>C	NP_001137462.1:p.Arg398Pro
NM_001143991.1:c.1193G>C	NP_001137463.1:p.Arg398Pro
NM_001143992.1:c.1193G>C	NP_001137464.1:p.Arg398Pro
NM_018081.2:c.1193G>C , LRG_375t1:c.1193G>C	NP_060551.2:p.Arg398Pro
XM_011523952.1:c.554G>C	XP_011522254.1:p.Arg185Pro
XM_011523952.2:c.554G>C	XP_011522254.1:p.Arg185Pro
XM_024450824.1:c.401G>C	XP_024306592.1:p.Arg134Pro
XR_001752551.2:n.1470G>C
NM_001143991.2:c.1193G>C	NP_001137463.1:p.Arg398Pro
NM_001143992.2:c.1193G>C MANE Select	NP_001137464.1:p.Arg398Pro
NM_001143990.2:c.1193G>C	NP_001137462.1:p.Arg398Pro