Canonical Allele Identifier: CA370916449

Gene: WRN

Linked Data

• MyVariant Identifiers: chr8:g.30924698T>A (hg19) ; chr8:g.31067182T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31067182T>A , CM000670.2:g.31067182T>A	GRCh38
NC_000008.10:g.30924698T>A , CM000670.1:g.30924698T>A	GRCh37
NC_000008.9:g.31044240T>A	NCBI36
NG_008870.1:g.38921T>A , LRG_524:g.38921T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298139.7:c.654T>A MANE Select	ENSP00000298139.5:p.Tyr218Ter
ENST00000650667.1:c.*268T>A	ENSP00000498593.1:n.*268T>A
ENST00000298139.5:c.654T>A	ENSP00000298139.5:p.Tyr218Ter
NM_000553.4:c.654T>A , LRG_524t1:c.654T>A	NP_000544.2:p.Tyr218Ter
XM_011544639.1:c.654T>A	XP_011542941.1:p.Tyr218Ter
XR_949470.1:n.927T>A
XR_949471.1:n.927T>A
XR_949472.1:n.927T>A
NM_000553.5:c.654T>A	NP_000544.2:p.Tyr218Ter
XM_011544639.3:c.654T>A	XP_011542941.1:p.Tyr218Ter
XM_024447265.1:c.444T>A	XP_024303033.1:p.Tyr148Ter
XR_949470.3:n.955T>A
XR_949471.3:n.955T>A
XR_949472.3:n.955T>A
NM_000553.6:c.654T>A MANE Select	NP_000544.2:p.Tyr218Ter