Canonical Allele Identifier: CA370916887

Gene: WRN

Linked Data

• MyVariant Identifiers: chr8:g.30925781T>A (hg19) ; chr8:g.31068265T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31068265T>A , CM000670.2:g.31068265T>A	GRCh38
NC_000008.10:g.30925781T>A , CM000670.1:g.30925781T>A	GRCh37
NC_000008.9:g.31045323T>A	NCBI36
NG_008870.1:g.40004T>A , LRG_524:g.40004T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000298139.7:c.662T>A MANE Select	ENSP00000298139.5:p.Phe221Tyr
ENST00000650667.1:c.*276T>A	ENSP00000498593.1:n.*276T>A
ENST00000298139.5:c.662T>A	ENSP00000298139.5:p.Phe221Tyr
NM_000553.4:c.662T>A , LRG_524t1:c.662T>A	NP_000544.2:p.Phe221Tyr
XM_011544639.1:c.662T>A	XP_011542941.1:p.Phe221Tyr
XR_949470.1:n.935T>A
XR_949471.1:n.935T>A
XR_949472.1:n.935T>A
NM_000553.5:c.662T>A	NP_000544.2:p.Phe221Tyr
XM_011544639.3:c.662T>A	XP_011542941.1:p.Phe221Tyr
XM_024447265.1:c.452T>A	XP_024303033.1:p.Phe151Tyr
XR_949470.3:n.963T>A
XR_949471.3:n.963T>A
XR_949472.3:n.963T>A
NM_000553.6:c.662T>A MANE Select	NP_000544.2:p.Phe221Tyr