Canonical Allele Identifier: CA645550060

Gene: WRN

Linked Data

• COSMIC: COSM5367737

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31067137dup , CM000670.2:g.31067137dup	GRCh38
NC_000008.10:g.30924653dup , CM000670.1:g.30924653dup	GRCh37
NC_000008.9:g.31044195dup	NCBI36
NG_008870.1:g.38876dup , LRG_524:g.38876dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298139.7:c.609dup MANE Select	ENSP00000298139.5:p.Pro204SerfsTer4
ENST00000650667.1:c.*223dup	ENSP00000498593.1:n.*223dup
ENST00000298139.5:c.609dup	ENSP00000298139.5:p.Pro204SerfsTer4
NM_000553.4:c.609dup , LRG_524t1:c.609dup	NP_000544.2:p.Pro204SerfsTer4
XM_011544639.1:c.609dup	XP_011542941.1:p.Pro204SerfsTer4
XR_949470.1:n.882dup
XR_949471.1:n.882dup
XR_949472.1:n.882dup
NM_000553.5:c.609dup	NP_000544.2:p.Pro204SerfsTer4
XM_011544639.3:c.609dup	XP_011542941.1:p.Pro204SerfsTer4
XM_024447265.1:c.399dup	XP_024303033.1:p.Pro134SerfsTer4
XR_949470.3:n.910dup
XR_949471.3:n.910dup
XR_949472.3:n.910dup
NM_000553.6:c.609dup MANE Select	NP_000544.2:p.Pro204SerfsTer4