Canonical Allele Identifier: CA162794
Gene: WRN HGNC NCBI

Linked Data

ClinVar Variation Id: 135448
dbSNP Id: rs148229804

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.31068323T>G , CM000670.2:g.31068323T>G GRCh38
NC_000008.10:g.30925839T>G , CM000670.1:g.30925839T>G GRCh37
NC_000008.9:g.31045381T>G NCBI36
NG_008870.1:g.40062T>G , LRG_524:g.40062T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000298139.7:c.720T>G MANE Select ENSP00000298139.5:p.Asn240Lys
ENST00000650667.1:c.*334T>G ENSP00000498593.1:p.=
ENST00000651642.1:n.15T>G ENSP00000498779.1:p.Asn5Lys
ENST00000298139.5:c.720T>G ENSP00000298139.5:p.Asn240Lys
NM_000553.4:c.720T>G , LRG_524t1:c.720T>G NP_000544.2:p.Asn240Lys
XM_011544639.1:c.720T>G XP_011542941.1:p.Asn240Lys
XR_949470.1:n.993T>G
XR_949471.1:n.993T>G
XR_949472.1:n.993T>G
NM_000553.5:c.720T>G NP_000544.2:p.Asn240Lys
XM_011544639.3:c.720T>G XP_011542941.1:p.Asn240Lys
XM_024447265.1:c.510T>G XP_024303033.1:p.Asn170Lys
XR_949470.3:n.1021T>G
XR_949471.3:n.1021T>G
XR_949472.3:n.1021T>G
NM_000553.6:c.720T>G MANE Select NP_000544.2:p.Asn240Lys