Canonical Allele Identifier: CA2580786844

Gene: WRN

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31081132C= , CM000670.2:g.31081132C=	GRCh38
NC_000008.10:g.30938648C= , CM000670.1:g.30938648C=	GRCh37
NC_000008.9:g.31058190C=	NCBI36
NG_008870.1:g.52871C= , LRG_524:g.52871C=

Transcript Alleles

HGVS	Amino-acid Change
NM_000553.6:c.1105C= MANE Select	NP_000544.2:p.Arg369=
ENST00000298139.7:c.1105C= MANE Select	ENSP00000298139.5:p.Arg369=
NM_000553.4:c.1105C= , LRG_524t1:c.1105C=	NP_000544.2:p.Arg369=
NM_000553.5:c.1105C=	NP_000544.2:p.Arg369=
ENST00000298139.5:c.1105C=	ENSP00000298139.5:p.Arg369=
ENST00000650667.1:c.*719C=	ENSP00000498593.1:n.*719C=
ENST00000651642.1:c.400C=	ENSP00000498779.1:p.Arg134=
XM_011544639.1:c.1105C=	XP_011542941.1:p.Arg369=
XM_011544639.3:c.1105C=	XP_011542941.1:p.Arg369=
XM_024447265.1:c.895C=	XP_024303033.1:p.Arg299=
XR_949470.1:n.1378C=
XR_949470.3:n.1406C=
XR_949471.1:n.1378C=
XR_949471.3:n.1406C=
XR_949472.1:n.1378C=
XR_949472.3:n.1406C=