Canonical Allele Identifier: CA370925319

Gene: WRN

Linked Data

• dbSNP Id: rs2130438692
• MyVariant Identifiers: chr8:g.31004601G>A (hg19) ; chr8:g.31147085G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31147085G>A , CM000670.2:g.31147085G>A	GRCh38
NC_000008.10:g.31004601G>A , CM000670.1:g.31004601G>A	GRCh37
NC_000008.9:g.31124143G>A	NCBI36
NG_008870.1:g.118824G>A , LRG_524:g.118824G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298139.7:c.3416G>A MANE Select	ENSP00000298139.5:p.Ser1139Asn
ENST00000650667.1:c.*3030G>A	ENSP00000498593.1:n.*3030G>A
ENST00000298139.5:c.3416G>A	ENSP00000298139.5:p.Ser1139Asn
ENST00000521620.5:n.2049G>A
NM_000553.4:c.3416G>A , LRG_524t1:c.3416G>A	NP_000544.2:p.Ser1139Asn
XM_011544639.1:c.3335G>A	XP_011542941.1:p.Ser1112Asn
XM_011544640.1:c.1817G>A	XP_011542942.1:p.Ser606Asn
XR_949470.1:n.3689G>A
XR_949471.1:n.3689G>A
XR_949472.1:n.3689G>A
XR_949643.1:n.614+1423C>T
NM_000553.5:c.3416G>A	NP_000544.2:p.Ser1139Asn
XM_011544639.3:c.3335G>A	XP_011542941.1:p.Ser1112Asn
XM_024447265.1:c.3206G>A	XP_024303033.1:p.Ser1069Asn
XR_949470.3:n.3717G>A
XR_949471.3:n.3717G>A
XR_949472.3:n.3717G>A
NM_000553.6:c.3416G>A MANE Select	NP_000544.2:p.Ser1139Asn