Canonical Allele Identifier: CA3156152472

Gene: WRN

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31064962A= , CM000670.2:g.31064962A=	GRCh38
NC_000008.10:g.30922478A= , CM000670.1:g.30922478A=	GRCh37
NC_000008.9:g.31042020A=	NCBI36
NG_008870.1:g.36701A= , LRG_524:g.36701A=

Transcript Alleles

HGVS	Amino-acid Change
NM_000553.6:c.403A= MANE Select	NP_000544.2:p.Lys135=
ENST00000298139.7:c.403A= MANE Select	ENSP00000298139.5:p.Lys135=
NM_000553.4:c.403A= , LRG_524t1:c.403A=	NP_000544.2:p.Lys135=
NM_000553.5:c.403A=	NP_000544.2:p.Lys135=
ENST00000298139.5:c.403A=	ENSP00000298139.5:p.Lys135=
ENST00000650667.1:c.*17A=	ENSP00000498593.1:n.*17A=
XM_011544639.1:c.403A=	XP_011542941.1:p.Lys135=
XM_011544639.3:c.403A=	XP_011542941.1:p.Lys135=
XM_024447265.1:c.193A=	XP_024303033.1:p.Lys65=
XR_949470.1:n.676A=
XR_949470.3:n.704A=
XR_949471.1:n.676A=
XR_949471.3:n.704A=
XR_949472.1:n.676A=
XR_949472.3:n.704A=