Canonical Allele Identifier: CA624729492

Gene: WRAP53

Linked Data

• dbSNP Id: rs1481819363
• gnomAD v2: 17-7591736-G-A
• gnomAD v3: 17-7688418-G-A
• gnomAD v4: 17-7688418-G-A
• MyVariant Identifiers: chr17:g.7591736G>A (hg19) ; chr17:g.7688418G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7688418G>A , CM000679.2:g.7688418G>A	GRCh38
NC_000017.10:g.7591736G>A , CM000679.1:g.7591736G>A	GRCh37
NC_000017.9:g.7532461G>A	NCBI36
NG_017013.2:g.4133C>T , LRG_321:g.4133C>T
NG_028245.1:g.7348G>A , LRG_375:g.7348G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698742.1:c.-145G>A	ENSP00000513904.1:n.-145G>A
ENST00000316024.9:c.-231G>A	ENSP00000324203.5:n.-231G>A
ENST00000396463.6:c.-145G>A	ENSP00000379727.2:n.-145G>A
ENST00000431639.6:c.-1-230G>A	ENSP00000397219.2:n.-1-230G>A
ENST00000457584.6:c.-1-230G>A	ENSP00000411061.2:n.-1-230G>A
ENST00000498311.5:c.-145G>A	ENSP00000432991.1:n.-145G>A
NM_001143990.1:c.-1-230G>A	NP_001137462.1:n.-1-230G>A
NM_001143991.1:c.-1-230G>A	NP_001137463.1:n.-1-230G>A
NM_001143992.1:c.-145G>A	NP_001137464.1:n.-145G>A
NM_018081.2:c.-231G>A , LRG_375t1:c.-231G>A	NP_060551.2:n.-231G>A
XM_024450825.1:c.-145G>A	XP_024306593.1:n.-145G>A
XR_001752551.2:n.101G>A
NM_001143991.2:c.-1-230G>A	NP_001137463.1:n.-1-230G>A
NM_001143990.2:c.-1-230G>A	NP_001137462.1:n.-1-230G>A