Canonical Allele Identifier: CA370918408

Gene: WRN

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31076202A>T , CM000670.2:g.31076202A>T	GRCh38
NC_000008.10:g.30933718A>T , CM000670.1:g.30933718A>T	GRCh37
NC_000008.9:g.31053260A>T	NCBI36
NG_008870.1:g.47941A>T , LRG_524:g.47941A>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000553.6:c.754A>T MANE Select	NP_000544.2:p.Lys252Ter
ENST00000298139.7:c.754A>T MANE Select	ENSP00000298139.5:p.Lys252Ter
NM_000553.4:c.754A>T , LRG_524t1:c.754A>T	NP_000544.2:p.Lys252Ter
NM_000553.5:c.754A>T	NP_000544.2:p.Lys252Ter
ENST00000298139.5:c.754A>T	ENSP00000298139.5:p.Lys252Ter
ENST00000650667.1:c.*368A>T	ENSP00000498593.1:n.*368A>T
ENST00000651642.1:c.49A>T	ENSP00000498779.1:p.Lys17Ter
XM_011544639.1:c.754A>T	XP_011542941.1:p.Lys252Ter
XM_011544639.3:c.754A>T	XP_011542941.1:p.Lys252Ter
XM_024447265.1:c.544A>T	XP_024303033.1:p.Lys182Ter
XR_949470.1:n.1027A>T
XR_949470.3:n.1055A>T
XR_949471.1:n.1027A>T
XR_949471.3:n.1055A>T
XR_949472.1:n.1027A>T
XR_949472.3:n.1055A>T