Canonical Allele Identifier: CA370917023

Gene: WRN

Linked Data

• MyVariant Identifiers: chr8:g.30925805T>C (hg19) ; chr8:g.31068289T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31068289T>C , CM000670.2:g.31068289T>C	GRCh38
NC_000008.10:g.30925805T>C , CM000670.1:g.30925805T>C	GRCh37
NC_000008.9:g.31045347T>C	NCBI36
NG_008870.1:g.40028T>C , LRG_524:g.40028T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298139.7:c.686T>C MANE Select	ENSP00000298139.5:p.Ile229Thr
ENST00000650667.1:c.*300T>C	ENSP00000498593.1:n.*300T>C
ENST00000298139.5:c.686T>C	ENSP00000298139.5:p.Ile229Thr
NM_000553.4:c.686T>C , LRG_524t1:c.686T>C	NP_000544.2:p.Ile229Thr
XM_011544639.1:c.686T>C	XP_011542941.1:p.Ile229Thr
XR_949470.1:n.959T>C
XR_949471.1:n.959T>C
XR_949472.1:n.959T>C
NM_000553.5:c.686T>C	NP_000544.2:p.Ile229Thr
XM_011544639.3:c.686T>C	XP_011542941.1:p.Ile229Thr
XM_024447265.1:c.476T>C	XP_024303033.1:p.Ile159Thr
XR_949470.3:n.987T>C
XR_949471.3:n.987T>C
XR_949472.3:n.987T>C
NM_000553.6:c.686T>C MANE Select	NP_000544.2:p.Ile229Thr