Canonical Allele Identifier: CA370916878

Gene: WRN

Linked Data

• MyVariant Identifiers: chr8:g.30925778G>A (hg19) ; chr8:g.31068262G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31068262G>A , CM000670.2:g.31068262G>A	GRCh38
NC_000008.10:g.30925778G>A , CM000670.1:g.30925778G>A	GRCh37
NC_000008.9:g.31045320G>A	NCBI36
NG_008870.1:g.40001G>A , LRG_524:g.40001G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000298139.7:c.659G>A MANE Select	ENSP00000298139.5:p.Gly220Asp
ENST00000650667.1:c.*273G>A	ENSP00000498593.1:n.*273G>A
ENST00000298139.5:c.659G>A	ENSP00000298139.5:p.Gly220Asp
NM_000553.4:c.659G>A , LRG_524t1:c.659G>A	NP_000544.2:p.Gly220Asp
XM_011544639.1:c.659G>A	XP_011542941.1:p.Gly220Asp
XR_949470.1:n.932G>A
XR_949471.1:n.932G>A
XR_949472.1:n.932G>A
NM_000553.5:c.659G>A	NP_000544.2:p.Gly220Asp
XM_011544639.3:c.659G>A	XP_011542941.1:p.Gly220Asp
XM_024447265.1:c.449G>A	XP_024303033.1:p.Gly150Asp
XR_949470.3:n.960G>A
XR_949471.3:n.960G>A
XR_949472.3:n.960G>A
NM_000553.6:c.659G>A MANE Select	NP_000544.2:p.Gly220Asp