Canonical Allele Identifier: CA2779595765

Gene: WRN

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31068120_31068121dup , CM000670.2:g.31068120_31068121dup	GRCh38
NC_000008.10:g.30925636_30925637dup , CM000670.1:g.30925636_30925637dup	GRCh37
NC_000008.9:g.31045178_31045179dup	NCBI36
NG_008870.1:g.39859_39860dup , LRG_524:g.39859_39860dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298139.7:c.655-138_655-137dup MANE Select	ENSP00000298139.5:n.655-138_655-137dup
ENST00000650667.1:c.*269-138_*269-137dup	ENSP00000498593.1:n.*269-138_*269-137dup
ENST00000298139.5:c.655-138_655-137dup	ENSP00000298139.5:n.655-138_655-137dup
NM_000553.4:c.655-138_655-137dup , LRG_524t1:c.655-138_655-137dup	NP_000544.2:n.655-138_655-137dup
XM_011544639.1:c.655-138_655-137dup	XP_011542941.1:n.655-138_655-137dup
XR_949470.1:n.928-138_928-137dup
XR_949471.1:n.928-138_928-137dup
XR_949472.1:n.928-138_928-137dup
NM_000553.5:c.655-138_655-137dup	NP_000544.2:n.655-138_655-137dup
XM_011544639.3:c.655-138_655-137dup	XP_011542941.1:n.655-138_655-137dup
XM_024447265.1:c.445-138_445-137dup	XP_024303033.1:n.445-138_445-137dup
XR_949470.3:n.956-138_956-137dup
XR_949471.3:n.956-138_956-137dup
XR_949472.3:n.956-138_956-137dup
NM_000553.6:c.655-138_655-137dup MANE Select	NP_000544.2:n.655-138_655-137dup