Canonical Allele Identifier: CA3156098677

Gene: WRN

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31157461C= , CM000670.2:g.31157461C=	GRCh38
NC_000008.10:g.31014977C= , CM000670.1:g.31014977C=	GRCh37
NC_000008.9:g.31134519C=	NCBI36
NG_008870.1:g.129200C= , LRG_524:g.129200C=

Transcript Alleles

HGVS	Amino-acid Change
NM_000553.6:c.3913C= MANE Select	NP_000544.2:p.Arg1305=
ENST00000298139.7:c.3913C= MANE Select	ENSP00000298139.5:p.Arg1305=
NM_000553.4:c.3913C= , LRG_524t1:c.3913C=	NP_000544.2:p.Arg1305=
NM_000553.5:c.3913C=	NP_000544.2:p.Arg1305=
ENST00000298139.5:c.3913C=	ENSP00000298139.5:p.Arg1305=
ENST00000521620.5:n.2546C=
ENST00000650667.1:c.*3527C=	ENSP00000498593.1:n.*3527C=
XM_011544639.1:c.3832C=	XP_011542941.1:p.Arg1278=
XM_011544639.3:c.3832C=	XP_011542941.1:p.Arg1278=
XM_011544640.1:c.2314C=	XP_011542942.1:p.Arg772=
XM_024447265.1:c.3703C=	XP_024303033.1:p.Arg1235=
XR_949470.1:n.4186C=
XR_949470.3:n.4214C=
XR_949471.1:n.4186C=
XR_949471.3:n.4214C=
XR_949472.1:n.4186C=
XR_949472.3:n.4214C=
XR_949643.1:n.457-8796G=
XR_949644.1:n.381-8796G=
XR_949647.1:n.1070-8796G=
XR_949648.1:n.972-8796G=