Canonical Allele Identifier: CA370912606

Gene: WRN

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31059227C>G , CM000670.2:g.31059227C>G	GRCh38
NC_000008.10:g.30916743C>G , CM000670.1:g.30916743C>G	GRCh37
NC_000008.9:g.31036285C>G	NCBI36
NG_008870.1:g.30966C>G , LRG_524:g.30966C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000553.6:c.171C>G MANE Select	NP_000544.2:p.Tyr57Ter
ENST00000298139.7:c.171C>G MANE Select	ENSP00000298139.5:p.Tyr57Ter
NM_000553.4:c.171C>G , LRG_524t1:c.171C>G	NP_000544.2:p.Tyr57Ter
NM_000553.5:c.171C>G	NP_000544.2:p.Tyr57Ter
ENST00000298139.5:c.171C>G	ENSP00000298139.5:p.Tyr57Ter
ENST00000650667.1:c.171C>G	ENSP00000498593.1:p.Tyr57Ter
XM_011544639.1:c.171C>G	XP_011542941.1:p.Tyr57Ter
XM_011544639.3:c.171C>G	XP_011542941.1:p.Tyr57Ter
XM_024447265.1:c.-164C>G	XP_024303033.1:n.-164C>G
XR_949470.1:n.444C>G
XR_949470.3:n.472C>G
XR_949471.1:n.444C>G
XR_949471.3:n.472C>G
XR_949472.1:n.444C>G
XR_949472.3:n.472C>G