Canonical Allele Identifier: CA460219822

Gene: WRN

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31064934A>G , CM000670.2:g.31064934A>G	GRCh38
NC_000008.10:g.30922450A>G , CM000670.1:g.30922450A>G	GRCh37
NC_000008.9:g.31041992A>G	NCBI36
NG_008870.1:g.36673A>G , LRG_524:g.36673A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000553.6:c.375A>G MANE Select	NP_000544.2:p.Lys125=
ENST00000298139.7:c.375A>G MANE Select	ENSP00000298139.5:p.Lys125=
NM_000553.4:c.375A>G , LRG_524t1:c.375A>G	NP_000544.2:p.Lys125=
NM_000553.5:c.375A>G	NP_000544.2:p.Lys125=
ENST00000298139.5:c.375A>G	ENSP00000298139.5:p.Lys125=
ENST00000650667.1:c.229A>G	ENSP00000498593.1:p.Asn77Asp
XM_011544639.1:c.375A>G	XP_011542941.1:p.Lys125=
XM_011544639.3:c.375A>G	XP_011542941.1:p.Lys125=
XM_024447265.1:c.165A>G	XP_024303033.1:p.Lys55=
XR_949470.1:n.648A>G
XR_949470.3:n.676A>G
XR_949471.1:n.648A>G
XR_949471.3:n.676A>G
XR_949472.1:n.648A>G
XR_949472.3:n.676A>G