Canonical Allele Identifier: CA4704228

Gene: WRN

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31080988G>T , CM000670.2:g.31080988G>T	GRCh38
NC_000008.10:g.30938504G>T , CM000670.1:g.30938504G>T	GRCh37
NC_000008.9:g.31058046G>T	NCBI36
NG_008870.1:g.52727G>T , LRG_524:g.52727G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000553.6:c.961G>T MANE Select	NP_000544.2:p.Glu321Ter
ENST00000298139.7:c.961G>T MANE Select	ENSP00000298139.5:p.Glu321Ter
NM_000553.4:c.961G>T , LRG_524t1:c.961G>T	NP_000544.2:p.Glu321Ter
NM_000553.5:c.961G>T	NP_000544.2:p.Glu321Ter
ENST00000298139.5:c.961G>T	ENSP00000298139.5:p.Glu321Ter
ENST00000650667.1:c.*575G>T	ENSP00000498593.1:n.*575G>T
ENST00000651642.1:c.256G>T	ENSP00000498779.1:p.Glu86Ter
XM_011544639.1:c.961G>T	XP_011542941.1:p.Glu321Ter
XM_011544639.3:c.961G>T	XP_011542941.1:p.Glu321Ter
XM_024447265.1:c.751G>T	XP_024303033.1:p.Glu251Ter
XR_949470.1:n.1234G>T
XR_949470.3:n.1262G>T
XR_949471.1:n.1234G>T
XR_949471.3:n.1262G>T
XR_949472.1:n.1234G>T
XR_949472.3:n.1262G>T