Canonical Allele Identifier: CA370922846

Gene: WRN

Linked Data

• MyVariant Identifiers: chr8:g.30999204A>T (hg19) ; chr8:g.31141688A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31141688A>T , CM000670.2:g.31141688A>T	GRCh38
NC_000008.10:g.30999204A>T , CM000670.1:g.30999204A>T	GRCh37
NC_000008.9:g.31118746A>T	NCBI36
NG_008870.1:g.113427A>T , LRG_524:g.113427A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298139.7:c.3146A>T MANE Select	ENSP00000298139.5:p.Asn1049Ile
ENST00000650667.1:c.*2760A>T	ENSP00000498593.1:n.*2760A>T
ENST00000298139.5:c.3146A>T	ENSP00000298139.5:p.Asn1049Ile
ENST00000521620.5:n.1779A>T
NM_000553.4:c.3146A>T , LRG_524t1:c.3146A>T	NP_000544.2:p.Asn1049Ile
XM_011544639.1:c.3065A>T	XP_011542941.1:p.Asn1022Ile
XM_011544640.1:c.1547A>T	XP_011542942.1:p.Asn516Ile
XR_949470.1:n.3419A>T
XR_949471.1:n.3419A>T
XR_949472.1:n.3419A>T
NM_000553.5:c.3146A>T	NP_000544.2:p.Asn1049Ile
XM_011544639.3:c.3065A>T	XP_011542941.1:p.Asn1022Ile
XM_024447265.1:c.2936A>T	XP_024303033.1:p.Asn979Ile
XR_949470.3:n.3447A>T
XR_949471.3:n.3447A>T
XR_949472.3:n.3447A>T
NM_000553.6:c.3146A>T MANE Select	NP_000544.2:p.Asn1049Ile