Canonical Allele Identifier: CA162758

Gene: WRN

Linked Data

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31154721C>G , CM000670.2:g.31154721C>G	GRCh38
NC_000008.10:g.31012237C>G , CM000670.1:g.31012237C>G	GRCh37
NC_000008.9:g.31131779C>G	NCBI36
NG_008870.1:g.126460C>G , LRG_524:g.126460C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298139.7:c.3785C>G MANE Select	ENSP00000298139.5:p.Thr1262Arg
ENST00000650667.1:c.*3399C>G	ENSP00000498593.1:n.*3399C>G
ENST00000298139.5:c.3785C>G	ENSP00000298139.5:p.Thr1262Arg
ENST00000521620.5:n.2418C>G
NM_000553.4:c.3785C>G , LRG_524t1:c.3785C>G	NP_000544.2:p.Thr1262Arg
XM_011544639.1:c.3704C>G	XP_011542941.1:p.Thr1235Arg
XM_011544640.1:c.2186C>G	XP_011542942.1:p.Thr729Arg
XR_949470.1:n.4058C>G
XR_949471.1:n.4058C>G
XR_949472.1:n.4058C>G
XR_949643.1:n.457-6056G>C
XR_949644.1:n.381-6056G>C
XR_949647.1:n.1070-6056G>C
XR_949648.1:n.972-6056G>C
NM_000553.5:c.3785C>G	NP_000544.2:p.Thr1262Arg
XM_011544639.3:c.3704C>G	XP_011542941.1:p.Thr1235Arg
XM_024447265.1:c.3575C>G	XP_024303033.1:p.Thr1192Arg
XR_949470.3:n.4086C>G
XR_949471.3:n.4086C>G
XR_949472.3:n.4086C>G
NM_000553.6:c.3785C>G MANE Select	NP_000544.2:p.Thr1262Arg