Canonical Allele Identifier: CA370913394

Gene: WRN

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31116370G>T , CM000670.2:g.31116370G>T	GRCh38
NC_000008.10:g.30973886G>T , CM000670.1:g.30973886G>T	GRCh37
NC_000008.9:g.31093428G>T	NCBI36
NG_008870.1:g.88109G>T , LRG_524:g.88109G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000553.6:c.2290G>T MANE Select	NP_000544.2:p.Glu764Ter
ENST00000298139.7:c.2290G>T MANE Select	ENSP00000298139.5:p.Glu764Ter
NM_000553.4:c.2290G>T , LRG_524t1:c.2290G>T	NP_000544.2:p.Glu764Ter
NM_000553.5:c.2290G>T	NP_000544.2:p.Glu764Ter
ENST00000298139.5:c.2290G>T	ENSP00000298139.5:p.Glu764Ter
ENST00000521620.5:n.923G>T
ENST00000650667.1:c.*1904G>T	ENSP00000498593.1:n.*1904G>T
XM_011544639.1:c.2209G>T	XP_011542941.1:p.Glu737Ter
XM_011544639.3:c.2209G>T	XP_011542941.1:p.Glu737Ter
XM_011544640.1:c.691G>T	XP_011542942.1:p.Glu231Ter
XM_024447265.1:c.2080G>T	XP_024303033.1:p.Glu694Ter
XR_949470.1:n.2563G>T
XR_949470.3:n.2591G>T
XR_949471.1:n.2563G>T
XR_949471.3:n.2591G>T
XR_949472.1:n.2563G>T
XR_949472.3:n.2591G>T