Canonical Allele Identifier: CA2839135560

Gene: WRN

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31033932T>A , CM000670.2:g.31033932T>A	GRCh38
NC_000008.10:g.30891448T>A , CM000670.1:g.30891448T>A	GRCh37
NC_000008.9:g.31010990T>A	NCBI36
NG_008870.1:g.5671T>A , LRG_524:g.5671T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298139.7:c.-118T>A MANE Select	ENSP00000298139.5:n.-118T>A
ENST00000650667.1:c.-118T>A	ENSP00000498593.1:n.-118T>A
ENST00000298139.5:c.-118T>A	ENSP00000298139.5:n.-118T>A
NM_000553.4:c.-118T>A , LRG_524t1:c.-118T>A	NP_000544.2:n.-118T>A
XM_011544639.1:c.-118T>A	XP_011542941.1:n.-118T>A
XR_949470.1:n.156T>A
XR_949471.1:n.156T>A
XR_949472.1:n.156T>A
NM_000553.5:c.-118T>A	NP_000544.2:n.-118T>A
XM_011544639.3:c.-118T>A	XP_011542941.1:n.-118T>A
XM_024447265.1:c.-452T>A	XP_024303033.1:n.-452T>A
XR_949470.3:n.184T>A
XR_949471.3:n.184T>A
XR_949472.3:n.184T>A
NM_000553.6:c.-118T>A MANE Select	NP_000544.2:n.-118T>A