Canonical Allele Identifier: CA2580814477

Gene: WRN

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31043374A= , CM000670.2:g.31043374A=	GRCh38
NC_000008.10:g.30900890A= , CM000670.1:g.30900890A=	GRCh37
NC_000008.9:g.31020432A=	NCBI36
NG_008870.1:g.15113A= , LRG_524:g.15113A=

Transcript Alleles

HGVS	Amino-acid Change
NM_000553.6:c.-77+9401A= MANE Select	NP_000544.2:n.-77+9401A=
ENST00000298139.7:c.-77+9401A= MANE Select	ENSP00000298139.5:n.-77+9401A=
NM_000553.4:c.-77+9401A= , LRG_524t1:c.-77+9401A=	NP_000544.2:n.-77+9401A=
NM_000553.5:c.-77+9401A=	NP_000544.2:n.-77+9401A=
ENST00000298139.5:c.-77+9401A=	ENSP00000298139.5:n.-77+9401A=
ENST00000650667.1:c.-77+9401A=	ENSP00000498593.1:n.-77+9401A=
XM_011544639.1:c.-77+9401A=	XP_011542941.1:n.-77+9401A=
XM_011544639.3:c.-77+9401A=	XP_011542941.1:n.-77+9401A=
XM_024447265.1:c.-411+9401A=	XP_024303033.1:n.-411+9401A=
XR_949470.1:n.197+9401A=
XR_949470.3:n.225+9401A=
XR_949471.1:n.197+9401A=
XR_949471.3:n.225+9401A=
XR_949472.1:n.197+9401A=
XR_949472.3:n.225+9401A=