Canonical Allele Identifier: CA370925796

Gene: WRN

Linked Data

• MyVariant Identifiers: chr8:g.31004922G>A (hg19) ; chr8:g.31147406G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31147406G>A , CM000670.2:g.31147406G>A	GRCh38
NC_000008.10:g.31004922G>A , CM000670.1:g.31004922G>A	GRCh37
NC_000008.9:g.31124464G>A	NCBI36
NG_008870.1:g.119145G>A , LRG_524:g.119145G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298139.7:c.3502G>A MANE Select	ENSP00000298139.5:p.Ala1168Thr
ENST00000650667.1:c.*3116G>A	ENSP00000498593.1:n.*3116G>A
ENST00000298139.5:c.3502G>A	ENSP00000298139.5:p.Ala1168Thr
ENST00000521620.5:n.2135G>A
NM_000553.4:c.3502G>A , LRG_524t1:c.3502G>A	NP_000544.2:p.Ala1168Thr
XM_011544639.1:c.3421G>A	XP_011542941.1:p.Ala1141Thr
XM_011544640.1:c.1903G>A	XP_011542942.1:p.Ala635Thr
XR_949470.1:n.3775G>A
XR_949471.1:n.3775G>A
XR_949472.1:n.3775G>A
XR_949643.1:n.614+1102C>T
NM_000553.5:c.3502G>A	NP_000544.2:p.Ala1168Thr
XM_011544639.3:c.3421G>A	XP_011542941.1:p.Ala1141Thr
XM_024447265.1:c.3292G>A	XP_024303033.1:p.Ala1098Thr
XR_949470.3:n.3803G>A
XR_949471.3:n.3803G>A
XR_949472.3:n.3803G>A
NM_000553.6:c.3502G>A MANE Select	NP_000544.2:p.Ala1168Thr