Canonical Allele Identifier: CA918233052

Gene: WRN

Linked Data

• dbSNP Id: rs1554532730

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31141608del , CM000670.2:g.31141608del	GRCh38
NC_000008.10:g.30999124del , CM000670.1:g.30999124del	GRCh37
NC_000008.9:g.31118666del	NCBI36
NG_008870.1:g.113347del , LRG_524:g.113347del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298139.7:c.3138+8del MANE Select	ENSP00000298139.5:n.3138+8del
ENST00000650667.1:c.*2752+8del	ENSP00000498593.1:n.*2752+8del
ENST00000298139.5:c.3138+8del	ENSP00000298139.5:n.3138+8del
ENST00000521620.5:n.1771+8del
NM_000553.4:c.3138+8del , LRG_524t1:c.3138+8del	NP_000544.2:n.3138+8del
XM_011544639.1:c.3057+8del	XP_011542941.1:n.3057+8del
XM_011544640.1:c.1539+8del	XP_011542942.1:n.1539+8del
XR_949470.1:n.3411+8del
XR_949471.1:n.3411+8del
XR_949472.1:n.3411+8del
NM_000553.5:c.3138+8del	NP_000544.2:n.3138+8del
XM_011544639.3:c.3057+8del	XP_011542941.1:n.3057+8del
XM_024447265.1:c.2928+8del	XP_024303033.1:n.2928+8del
XR_949470.3:n.3439+8del
XR_949471.3:n.3439+8del
XR_949472.3:n.3439+8del
NM_000553.6:c.3138+8del MANE Select	NP_000544.2:n.3138+8del