Canonical Allele Identifier: CA4704042

Gene: WRN

Linked Data

• ClinVar Variation Id: 256709
• ClinVar RCV Id: RCV000247141 ; RCV001618394 ; RCV002057396 ; RCV003316351
• dbSNP Id: rs4987239
• ExAC: 8:30921970 A / T
• gnomAD v2: 8-30921970-A-T
• gnomAD v3: 8-31064454-A-T
• gnomAD v4: 8-31064454-A-T
• MyVariant Identifiers: chr8:g.30921970A>T (hg19) ; chr8:g.31064454A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31064454A>T , CM000670.2:g.31064454A>T	GRCh38
NC_000008.10:g.30921970A>T , CM000670.1:g.30921970A>T	GRCh37
NC_000008.9:g.31041512A>T	NCBI36
NG_008870.1:g.36193A>T , LRG_524:g.36193A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298139.7:c.355+20A>T MANE Select	ENSP00000298139.5:n.355+20A>T
ENST00000650667.1:c.210-461A>T	ENSP00000498593.1:n.210-461A>T
ENST00000298139.5:c.355+20A>T	ENSP00000298139.5:n.355+20A>T
NM_000553.4:c.355+20A>T , LRG_524t1:c.355+20A>T	NP_000544.2:n.355+20A>T
XM_011544639.1:c.355+20A>T	XP_011542941.1:n.355+20A>T
XR_949470.1:n.628+20A>T
XR_949471.1:n.628+20A>T
XR_949472.1:n.628+20A>T
NM_000553.5:c.355+20A>T	NP_000544.2:n.355+20A>T
XM_011544639.3:c.355+20A>T	XP_011542941.1:n.355+20A>T
XM_024447265.1:c.145+20A>T	XP_024303033.1:n.145+20A>T
XR_949470.3:n.656+20A>T
XR_949471.3:n.656+20A>T
XR_949472.3:n.656+20A>T
NM_000553.6:c.355+20A>T MANE Select	NP_000544.2:n.355+20A>T