Canonical Allele Identifier: CA370928838

Gene: WRN

Linked Data

• MyVariant Identifiers: chr8:g.31012145C>G (hg19) ; chr8:g.31154629C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31154629C>G , CM000670.2:g.31154629C>G	GRCh38
NC_000008.10:g.31012145C>G , CM000670.1:g.31012145C>G	GRCh37
NC_000008.9:g.31131687C>G	NCBI36
NG_008870.1:g.126368C>G , LRG_524:g.126368C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000298139.7:c.3693C>G MANE Select	ENSP00000298139.5:p.Asp1231Glu
ENST00000650667.1:c.*3307C>G	ENSP00000498593.1:n.*3307C>G
ENST00000298139.5:c.3693C>G	ENSP00000298139.5:p.Asp1231Glu
ENST00000521620.5:n.2326C>G
NM_000553.4:c.3693C>G , LRG_524t1:c.3693C>G	NP_000544.2:p.Asp1231Glu
XM_011544639.1:c.3612C>G	XP_011542941.1:p.Asp1204Glu
XM_011544640.1:c.2094C>G	XP_011542942.1:p.Asp698Glu
XR_949470.1:n.3966C>G
XR_949471.1:n.3966C>G
XR_949472.1:n.3966C>G
XR_949643.1:n.457-5964G>C
XR_949644.1:n.381-5964G>C
XR_949647.1:n.1070-5964G>C
XR_949648.1:n.972-5964G>C
NM_000553.5:c.3693C>G	NP_000544.2:p.Asp1231Glu
XM_011544639.3:c.3612C>G	XP_011542941.1:p.Asp1204Glu
XM_024447265.1:c.3483C>G	XP_024303033.1:p.Asp1161Glu
XR_949470.3:n.3994C>G
XR_949471.3:n.3994C>G
XR_949472.3:n.3994C>G
NM_000553.6:c.3693C>G MANE Select	NP_000544.2:p.Asp1231Glu