Canonical Allele Identifier: CA162722

Gene: WRN

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31132476T>G , CM000670.2:g.31132476T>G	GRCh38
NC_000008.10:g.30989992T>G , CM000670.1:g.30989992T>G	GRCh37
NC_000008.9:g.31109534T>G	NCBI36
NG_008870.1:g.104215T>G , LRG_524:g.104215T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298139.7:c.2937T>G MANE Select	ENSP00000298139.5:p.Ile979Met
ENST00000650667.1:c.*2551T>G	ENSP00000498593.1:n.*2551T>G
ENST00000298139.5:c.2937T>G	ENSP00000298139.5:p.Ile979Met
ENST00000521620.5:n.1570T>G
NM_000553.4:c.2937T>G , LRG_524t1:c.2937T>G	NP_000544.2:p.Ile979Met
XM_011544639.1:c.2856T>G	XP_011542941.1:p.Ile952Met
XM_011544640.1:c.1338T>G	XP_011542942.1:p.Ile446Met
XR_949470.1:n.3210T>G
XR_949471.1:n.3210T>G
XR_949472.1:n.3210T>G
NM_000553.5:c.2937T>G	NP_000544.2:p.Ile979Met
XM_011544639.3:c.2856T>G	XP_011542941.1:p.Ile952Met
XM_024447265.1:c.2727T>G	XP_024303033.1:p.Ile909Met
XR_949470.3:n.3238T>G
XR_949471.3:n.3238T>G
XR_949472.3:n.3238T>G
NM_000553.6:c.2937T>G MANE Select	NP_000544.2:p.Ile979Met