Canonical Allele Identifier: CA370913480

Gene: WRN

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31116393T>G , CM000670.2:g.31116393T>G	GRCh38
NC_000008.10:g.30973909T>G , CM000670.1:g.30973909T>G	GRCh37
NC_000008.9:g.31093451T>G	NCBI36
NG_008870.1:g.88132T>G , LRG_524:g.88132T>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000553.6:c.2313T>G MANE Select	NP_000544.2:p.Cys771Trp
ENST00000298139.7:c.2313T>G MANE Select	ENSP00000298139.5:p.Cys771Trp
NM_000553.4:c.2313T>G , LRG_524t1:c.2313T>G	NP_000544.2:p.Cys771Trp
NM_000553.5:c.2313T>G	NP_000544.2:p.Cys771Trp
ENST00000298139.5:c.2313T>G	ENSP00000298139.5:p.Cys771Trp
ENST00000521620.5:n.946T>G
ENST00000650667.1:c.*1927T>G	ENSP00000498593.1:n.*1927T>G
XM_011544639.1:c.2232T>G	XP_011542941.1:p.Cys744Trp
XM_011544639.3:c.2232T>G	XP_011542941.1:p.Cys744Trp
XM_011544640.1:c.714T>G	XP_011542942.1:p.Cys238Trp
XM_024447265.1:c.2103T>G	XP_024303033.1:p.Cys701Trp
XR_949470.1:n.2586T>G
XR_949470.3:n.2614T>G
XR_949471.1:n.2586T>G
XR_949471.3:n.2614T>G
XR_949472.1:n.2586T>G
XR_949472.3:n.2614T>G