Canonical Allele Identifier: CA2716940578

Gene: WRN

Linked Data

• dbSNP Id: rs2130057057

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31068343T>A , CM000670.2:g.31068343T>A	GRCh38
NC_000008.10:g.30925859T>A , CM000670.1:g.30925859T>A	GRCh37
NC_000008.9:g.31045401T>A	NCBI36
NG_008870.1:g.40082T>A , LRG_524:g.40082T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000298139.7:c.724+16T>A MANE Select	ENSP00000298139.5:n.724+16T>A
ENST00000650667.1:c.*338+16T>A	ENSP00000498593.1:n.*338+16T>A
ENST00000651642.1:c.19+16T>A	ENSP00000498779.1:n.19+16T>A
ENST00000298139.5:c.724+16T>A	ENSP00000298139.5:n.724+16T>A
NM_000553.4:c.724+16T>A , LRG_524t1:c.724+16T>A	NP_000544.2:n.724+16T>A
XM_011544639.1:c.724+16T>A	XP_011542941.1:n.724+16T>A
XR_949470.1:n.997+16T>A
XR_949471.1:n.997+16T>A
XR_949472.1:n.997+16T>A
NM_000553.5:c.724+16T>A	NP_000544.2:n.724+16T>A
XM_011544639.3:c.724+16T>A	XP_011542941.1:n.724+16T>A
XM_024447265.1:c.514+16T>A	XP_024303033.1:n.514+16T>A
XR_949470.3:n.1025+16T>A
XR_949471.3:n.1025+16T>A
XR_949472.3:n.1025+16T>A
NM_000553.6:c.724+16T>A MANE Select	NP_000544.2:n.724+16T>A