Canonical Allele Identifier: CA4705026

Gene: WRN

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31143615T>C , CM000670.2:g.31143615T>C	GRCh38
NC_000008.10:g.31001131T>C , CM000670.1:g.31001131T>C	GRCh37
NC_000008.9:g.31120673T>C	NCBI36
NG_008870.1:g.115354T>C , LRG_524:g.115354T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_000553.6:c.3375T>C MANE Select	NP_000544.2:p.Ser1125=
ENST00000298139.7:c.3375T>C MANE Select	ENSP00000298139.5:p.Ser1125=
NM_000553.4:c.3375T>C , LRG_524t1:c.3375T>C	NP_000544.2:p.Ser1125=
NM_000553.5:c.3375T>C	NP_000544.2:p.Ser1125=
ENST00000298139.5:c.3375T>C	ENSP00000298139.5:p.Ser1125=
ENST00000521620.5:n.2008T>C
ENST00000650667.1:c.*2989T>C	ENSP00000498593.1:n.*2989T>C
XM_011544639.1:c.3294T>C	XP_011542941.1:p.Ser1098=
XM_011544639.3:c.3294T>C	XP_011542941.1:p.Ser1098=
XM_011544640.1:c.1776T>C	XP_011542942.1:p.Ser592=
XM_024447265.1:c.3165T>C	XP_024303033.1:p.Ser1055=
XR_949470.1:n.3648T>C
XR_949470.3:n.3676T>C
XR_949471.1:n.3648T>C
XR_949471.3:n.3676T>C
XR_949472.1:n.3648T>C
XR_949472.3:n.3676T>C