Canonical Allele Identifier: CA370920739

Gene: WRN

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31081132C>G , CM000670.2:g.31081132C>G	GRCh38
NC_000008.10:g.30938648C>G , CM000670.1:g.30938648C>G	GRCh37
NC_000008.9:g.31058190C>G	NCBI36
NG_008870.1:g.52871C>G , LRG_524:g.52871C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000553.6:c.1105C>G MANE Select	NP_000544.2:p.Arg369Gly
ENST00000298139.7:c.1105C>G MANE Select	ENSP00000298139.5:p.Arg369Gly
NM_000553.4:c.1105C>G , LRG_524t1:c.1105C>G	NP_000544.2:p.Arg369Gly
NM_000553.5:c.1105C>G	NP_000544.2:p.Arg369Gly
ENST00000298139.5:c.1105C>G	ENSP00000298139.5:p.Arg369Gly
ENST00000650667.1:c.*719C>G	ENSP00000498593.1:n.*719C>G
ENST00000651642.1:c.400C>G	ENSP00000498779.1:p.Arg134Gly
XM_011544639.1:c.1105C>G	XP_011542941.1:p.Arg369Gly
XM_011544639.3:c.1105C>G	XP_011542941.1:p.Arg369Gly
XM_024447265.1:c.895C>G	XP_024303033.1:p.Arg299Gly
XR_949470.1:n.1378C>G
XR_949470.3:n.1406C>G
XR_949471.1:n.1378C>G
XR_949471.3:n.1406C>G
XR_949472.1:n.1378C>G
XR_949472.3:n.1406C>G