Canonical Allele Identifier: CA370922362

Gene: WRN

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31141564T>G , CM000670.2:g.31141564T>G	GRCh38
NC_000008.10:g.30999080T>G , CM000670.1:g.30999080T>G	GRCh37
NC_000008.9:g.31118622T>G	NCBI36
NG_008870.1:g.113303T>G , LRG_524:g.113303T>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000553.6:c.3102T>G MANE Select	NP_000544.2:p.Tyr1034Ter
ENST00000298139.7:c.3102T>G MANE Select	ENSP00000298139.5:p.Tyr1034Ter
NM_000553.4:c.3102T>G , LRG_524t1:c.3102T>G	NP_000544.2:p.Tyr1034Ter
NM_000553.5:c.3102T>G	NP_000544.2:p.Tyr1034Ter
ENST00000298139.5:c.3102T>G	ENSP00000298139.5:p.Tyr1034Ter
ENST00000521620.5:n.1735T>G
ENST00000650667.1:c.*2716T>G	ENSP00000498593.1:n.*2716T>G
XM_011544639.1:c.3021T>G	XP_011542941.1:p.Tyr1007Ter
XM_011544639.3:c.3021T>G	XP_011542941.1:p.Tyr1007Ter
XM_011544640.1:c.1503T>G	XP_011542942.1:p.Tyr501Ter
XM_024447265.1:c.2892T>G	XP_024303033.1:p.Tyr964Ter
XR_949470.1:n.3375T>G
XR_949470.3:n.3403T>G
XR_949471.1:n.3375T>G
XR_949471.3:n.3403T>G
XR_949472.1:n.3375T>G
XR_949472.3:n.3403T>G