Canonical Allele Identifier: CA370924382

Gene: WRN

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31087828T>G , CM000670.2:g.31087828T>G	GRCh38
NC_000008.10:g.30945344T>G , CM000670.1:g.30945344T>G	GRCh37
NC_000008.9:g.31064886T>G	NCBI36
NG_008870.1:g.59567T>G , LRG_524:g.59567T>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000553.6:c.1484T>G MANE Select	NP_000544.2:p.Leu495Ter
ENST00000298139.7:c.1484T>G MANE Select	ENSP00000298139.5:p.Leu495Ter
NM_000553.4:c.1484T>G , LRG_524t1:c.1484T>G	NP_000544.2:p.Leu495Ter
NM_000553.5:c.1484T>G	NP_000544.2:p.Leu495Ter
ENST00000298139.5:c.1484T>G	ENSP00000298139.5:p.Leu495Ter
ENST00000521620.5:n.185T>G
ENST00000650667.1:c.*1098T>G	ENSP00000498593.1:n.*1098T>G
XM_011544639.1:c.1403T>G	XP_011542941.1:p.Leu468Ter
XM_011544639.3:c.1403T>G	XP_011542941.1:p.Leu468Ter
XM_011544640.1:c.-48T>G	XP_011542942.1:n.-48T>G
XM_024447265.1:c.1274T>G	XP_024303033.1:p.Leu425Ter
XR_949470.1:n.1757T>G
XR_949470.3:n.1785T>G
XR_949471.1:n.1757T>G
XR_949471.3:n.1785T>G
XR_949472.1:n.1757T>G
XR_949472.3:n.1785T>G