Canonical Allele Identifier: CA397855284

Gene: WRAP53

Linked Data

• ClinVar Variation Id: 2171536
• ClinVar RCV Id: RCV003086966
• dbSNP Id: rs2074056263
• gnomAD v4: 17-7688706-C-T
• MyVariant Identifiers: chr17:g.7592024C>T (hg19) ; chr17:g.7688706C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7688706C>T , CM000679.2:g.7688706C>T	GRCh38
NC_000017.10:g.7592024C>T , CM000679.1:g.7592024C>T	GRCh37
NC_000017.9:g.7532749C>T	NCBI36
NG_017013.2:g.3845G>A , LRG_321:g.3845G>A
NG_028245.1:g.7636C>T , LRG_375:g.7636C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698742.1:c.58C>T	ENSP00000513904.1:p.Pro20Ser
ENST00000698743.1:c.58C>T	ENSP00000513905.1:p.Pro20Ser
ENST00000698744.1:c.58C>T	ENSP00000513906.1:p.Pro20Ser
ENST00000698745.1:c.58C>T	ENSP00000513907.1:p.Pro20Ser
ENST00000698746.1:c.58C>T	ENSP00000513908.1:p.Pro20Ser
ENST00000396463.7:c.58C>T MANE Select	ENSP00000379727.3:p.Pro20Ser
ENST00000316024.9:c.58C>T	ENSP00000324203.5:p.Pro20Ser
ENST00000396463.6:c.58C>T	ENSP00000379727.2:p.Pro20Ser
ENST00000431639.6:c.58C>T	ENSP00000397219.2:p.Pro20Ser
ENST00000457584.6:c.58C>T	ENSP00000411061.2:p.Pro20Ser
ENST00000467699.5:n.144C>T
ENST00000498311.5:c.58C>T	ENSP00000432991.1:p.Pro20Ser
ENST00000534050.5:c.58C>T	ENSP00000434999.1:p.Pro20Ser
NM_001143990.1:c.58C>T	NP_001137462.1:p.Pro20Ser
NM_001143991.1:c.58C>T	NP_001137463.1:p.Pro20Ser
NM_001143992.1:c.58C>T	NP_001137464.1:p.Pro20Ser
NM_018081.2:c.58C>T , LRG_375t1:c.58C>T	NP_060551.2:p.Pro20Ser
XM_011523952.2:c.-575C>T	XP_011522254.1:n.-575C>T
XM_024450824.1:c.-2018C>T	XP_024306592.1:n.-2018C>T
XM_024450825.1:c.58C>T	XP_024306593.1:p.Pro20Ser
XR_001752551.2:n.303C>T
NM_001143991.2:c.58C>T	NP_001137463.1:p.Pro20Ser
NM_001143992.2:c.58C>T MANE Select	NP_001137464.1:p.Pro20Ser
NM_001143990.2:c.58C>T	NP_001137462.1:p.Pro20Ser