Canonical Allele Identifier: CA2779595769

Gene: WRN

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31068351A>T , CM000670.2:g.31068351A>T	GRCh38
NC_000008.10:g.30925867A>T , CM000670.1:g.30925867A>T	GRCh37
NC_000008.9:g.31045409A>T	NCBI36
NG_008870.1:g.40090A>T , LRG_524:g.40090A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298139.7:c.724+24A>T MANE Select	ENSP00000298139.5:n.724+24A>T
ENST00000650667.1:c.*338+24A>T	ENSP00000498593.1:n.*338+24A>T
ENST00000651642.1:c.19+24A>T	ENSP00000498779.1:n.19+24A>T
ENST00000298139.5:c.724+24A>T	ENSP00000298139.5:n.724+24A>T
NM_000553.4:c.724+24A>T , LRG_524t1:c.724+24A>T	NP_000544.2:n.724+24A>T
XM_011544639.1:c.724+24A>T	XP_011542941.1:n.724+24A>T
XR_949470.1:n.997+24A>T
XR_949471.1:n.997+24A>T
XR_949472.1:n.997+24A>T
NM_000553.5:c.724+24A>T	NP_000544.2:n.724+24A>T
XM_011544639.3:c.724+24A>T	XP_011542941.1:n.724+24A>T
XM_024447265.1:c.514+24A>T	XP_024303033.1:n.514+24A>T
XR_949470.3:n.1025+24A>T
XR_949471.3:n.1025+24A>T
XR_949472.3:n.1025+24A>T
NM_000553.6:c.724+24A>T MANE Select	NP_000544.2:n.724+24A>T