Canonical Allele Identifier: CA370925272

Gene: WRN

Linked Data

• MyVariant Identifiers: chr8:g.31004592A>G (hg19) ; chr8:g.31147076A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31147076A>G , CM000670.2:g.31147076A>G	GRCh38
NC_000008.10:g.31004592A>G , CM000670.1:g.31004592A>G	GRCh37
NC_000008.9:g.31124134A>G	NCBI36
NG_008870.1:g.118815A>G , LRG_524:g.118815A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298139.7:c.3407A>G MANE Select	ENSP00000298139.5:p.Lys1136Arg
ENST00000650667.1:c.*3021A>G	ENSP00000498593.1:n.*3021A>G
ENST00000298139.5:c.3407A>G	ENSP00000298139.5:p.Lys1136Arg
ENST00000521620.5:n.2040A>G
NM_000553.4:c.3407A>G , LRG_524t1:c.3407A>G	NP_000544.2:p.Lys1136Arg
XM_011544639.1:c.3326A>G	XP_011542941.1:p.Lys1109Arg
XM_011544640.1:c.1808A>G	XP_011542942.1:p.Lys603Arg
XR_949470.1:n.3680A>G
XR_949471.1:n.3680A>G
XR_949472.1:n.3680A>G
XR_949643.1:n.614+1432T>C
NM_000553.5:c.3407A>G	NP_000544.2:p.Lys1136Arg
XM_011544639.3:c.3326A>G	XP_011542941.1:p.Lys1109Arg
XM_024447265.1:c.3197A>G	XP_024303033.1:p.Lys1066Arg
XR_949470.3:n.3708A>G
XR_949471.3:n.3708A>G
XR_949472.3:n.3708A>G
NM_000553.6:c.3407A>G MANE Select	NP_000544.2:p.Lys1136Arg