Canonical Allele Identifier: CA1630835153

Gene: WRN

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31167138T= , CM000670.2:g.31167138T=	GRCh38
NC_000008.10:g.31024654T= , CM000670.1:g.31024654T=	GRCh37
NC_000008.9:g.31144196T=	NCBI36
NG_008870.1:g.138877T= , LRG_524:g.138877T=

Transcript Alleles

HGVS	Amino-acid Change
NM_000553.6:c.4099T= MANE Select	NP_000544.2:p.Cys1367=
ENST00000298139.7:c.4099T= MANE Select	ENSP00000298139.5:p.Cys1367=
NM_000553.4:c.4099T= , LRG_524t1:c.4099T=	NP_000544.2:p.Cys1367=
NM_000553.5:c.4099T=	NP_000544.2:p.Cys1367=
ENST00000298139.5:c.4099T=	ENSP00000298139.5:p.Cys1367=
ENST00000521620.5:n.2732T=
ENST00000650667.1:c.*3713T=	ENSP00000498593.1:n.*3713T=
ENST00000651946.1:n.323T=
XM_011544639.1:c.4018T=	XP_011542941.1:p.Cys1340=
XM_011544639.3:c.4018T=	XP_011542941.1:p.Cys1340=
XM_011544640.1:c.2500T=	XP_011542942.1:p.Cys834=
XM_024447265.1:c.3889T=	XP_024303033.1:p.Cys1297=
XR_949643.1:n.320A=
XR_949644.1:n.320A=
XR_949645.1:n.320A=
XR_949646.1:n.320A=
XR_949647.1:n.933A=
XR_949648.1:n.835A=