Canonical Allele Identifier: CA1630835150

Gene: WRN

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31141764G= , CM000670.2:g.31141764G=	GRCh38
NC_000008.10:g.30999280G= , CM000670.1:g.30999280G=	GRCh37
NC_000008.9:g.31118822G=	NCBI36
NG_008870.1:g.113503G= , LRG_524:g.113503G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298139.7:c.3222G= MANE Select	ENSP00000298139.5:p.Leu1074=
ENST00000650667.1:c.*2836G=	ENSP00000498593.1:n.*2836G=
ENST00000298139.5:c.3222G=	ENSP00000298139.5:p.Leu1074=
ENST00000521620.5:n.1855G=
NM_000553.4:c.3222G= , LRG_524t1:c.3222G=	NP_000544.2:p.Leu1074=
XM_011544639.1:c.3141G=	XP_011542941.1:p.Leu1047=
XM_011544640.1:c.1623G=	XP_011542942.1:p.Leu541=
XR_949470.1:n.3495G=
XR_949471.1:n.3495G=
XR_949472.1:n.3495G=
NM_000553.5:c.3222G=	NP_000544.2:p.Leu1074=
XM_011544639.3:c.3141G=	XP_011542941.1:p.Leu1047=
XM_024447265.1:c.3012G=	XP_024303033.1:p.Leu1004=
XR_949470.3:n.3523G=
XR_949471.3:n.3523G=
XR_949472.3:n.3523G=
NM_000553.6:c.3222G= MANE Select	NP_000544.2:p.Leu1074=