Canonical Allele Identifier: CA8354960

Gene: WRAP53

Linked Data

• ClinVar Variation Id: 325653
• ClinVar RCV Id: RCV000293257 ; RCV001518044
• dbSNP Id: rs17880740
• ExAC: 17:7592412 C / T
• gnomAD v2: 17-7592412-C-T
• gnomAD v3: 17-7689094-C-T
• gnomAD v4: 17-7689094-C-T
• MyVariant Identifiers: chr17:g.7592412C>T (hg19) ; chr17:g.7689094C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7689094C>T , CM000679.2:g.7689094C>T	GRCh38
NC_000017.10:g.7592412C>T , CM000679.1:g.7592412C>T	GRCh37
NC_000017.9:g.7533137C>T	NCBI36
NG_017013.2:g.3457G>A , LRG_321:g.3457G>A
NG_028245.1:g.8024C>T , LRG_375:g.8024C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698742.1:c.431+15C>T	ENSP00000513904.1:n.431+15C>T
ENST00000698743.1:c.431+15C>T	ENSP00000513905.1:n.431+15C>T
ENST00000698744.1:c.431+15C>T	ENSP00000513906.1:n.431+15C>T
ENST00000698745.1:c.431+15C>T	ENSP00000513907.1:n.431+15C>T
ENST00000698746.1:c.431+15C>T	ENSP00000513908.1:n.431+15C>T
ENST00000396463.7:c.431+15C>T MANE Select	ENSP00000379727.3:n.431+15C>T
ENST00000316024.9:c.431+15C>T	ENSP00000324203.5:n.431+15C>T
ENST00000396463.6:c.431+15C>T	ENSP00000379727.2:n.431+15C>T
ENST00000431639.6:c.431+15C>T	ENSP00000397219.2:n.431+15C>T
ENST00000457584.6:c.431+15C>T	ENSP00000411061.2:n.431+15C>T
ENST00000467699.5:n.517+15C>T
ENST00000498311.5:c.431+15C>T	ENSP00000432991.1:n.431+15C>T
ENST00000534050.5:c.431+15C>T	ENSP00000434999.1:n.431+15C>T
NM_001143990.1:c.431+15C>T	NP_001137462.1:n.431+15C>T
NM_001143991.1:c.431+15C>T	NP_001137463.1:n.431+15C>T
NM_001143992.1:c.431+15C>T	NP_001137464.1:n.431+15C>T
NM_018081.2:c.431+15C>T , LRG_375t1:c.431+15C>T	NP_060551.2:n.431+15C>T
XM_011523952.2:c.-202+15C>T	XP_011522254.1:n.-202+15C>T
XM_024450824.1:c.-1645+15C>T	XP_024306592.1:n.-1645+15C>T
XM_024450825.1:c.431+15C>T	XP_024306593.1:n.431+15C>T
XR_001752551.2:n.676+15C>T
NM_001143991.2:c.431+15C>T	NP_001137463.1:n.431+15C>T
NM_001143992.2:c.431+15C>T MANE Select	NP_001137464.1:n.431+15C>T
NM_001143990.2:c.431+15C>T	NP_001137462.1:n.431+15C>T