Canonical Allele Identifier: CA3156157383

Gene: WRN

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31068276C= , CM000670.2:g.31068276C=	GRCh38
NC_000008.10:g.30925792C= , CM000670.1:g.30925792C=	GRCh37
NC_000008.9:g.31045334C=	NCBI36
NG_008870.1:g.40015C= , LRG_524:g.40015C=

Transcript Alleles

HGVS	Amino-acid Change
NM_000553.6:c.673C= MANE Select	NP_000544.2:p.Arg225=
ENST00000298139.7:c.673C= MANE Select	ENSP00000298139.5:p.Arg225=
NM_000553.4:c.673C= , LRG_524t1:c.673C=	NP_000544.2:p.Arg225=
NM_000553.5:c.673C=	NP_000544.2:p.Arg225=
ENST00000298139.5:c.673C=	ENSP00000298139.5:p.Arg225=
ENST00000650667.1:c.*287C=	ENSP00000498593.1:n.*287C=
XM_011544639.1:c.673C=	XP_011542941.1:p.Arg225=
XM_011544639.3:c.673C=	XP_011542941.1:p.Arg225=
XM_024447265.1:c.463C=	XP_024303033.1:p.Arg155=
XR_949470.1:n.946C=
XR_949470.3:n.974C=
XR_949471.1:n.946C=
XR_949471.3:n.974C=
XR_949472.1:n.946C=
XR_949472.3:n.974C=