Canonical Allele Identifier: CA2686839691

Gene: WRN

Linked Data

• gnomAD v4: 8-31147173-A-AAC

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31147173_31147174insAC , CM000670.2:g.31147173_31147174insAC	GRCh38
NC_000008.10:g.31004689_31004690insAC , CM000670.1:g.31004689_31004690insAC	GRCh37
NC_000008.9:g.31124231_31124232insAC	NCBI36
NG_008870.1:g.118912_118913insAC , LRG_524:g.118912_118913insAC

Transcript Alleles

HGVS	Amino-acid change
ENST00000298139.7:c.3459+45_3459+46insAC MANE Select	ENSP00000298139.5:n.3459+45_3459+46insAC
ENST00000650667.1:c.*3073+45_*3073+46insAC	ENSP00000498593.1:n.*3073+45_*3073+46insAC
ENST00000298139.5:c.3459+45_3459+46insAC	ENSP00000298139.5:n.3459+45_3459+46insAC
ENST00000521620.5:n.2092+45_2092+46insAC
NM_000553.4:c.3459+45_3459+46insAC , LRG_524t1:c.3459+45_3459+46insAC	NP_000544.2:n.3459+45_3459+46insAC
XM_011544639.1:c.3378+45_3378+46insAC	XP_011542941.1:n.3378+45_3378+46insAC
XM_011544640.1:c.1860+45_1860+46insAC	XP_011542942.1:n.1860+45_1860+46insAC
XR_949470.1:n.3732+45_3732+46insAC
XR_949471.1:n.3732+45_3732+46insAC
XR_949472.1:n.3732+45_3732+46insAC
XR_949643.1:n.614+1334_614+1335insGT
NM_000553.5:c.3459+45_3459+46insAC	NP_000544.2:n.3459+45_3459+46insAC
XM_011544639.3:c.3378+45_3378+46insAC	XP_011542941.1:n.3378+45_3378+46insAC
XM_024447265.1:c.3249+45_3249+46insAC	XP_024303033.1:n.3249+45_3249+46insAC
XR_949470.3:n.3760+45_3760+46insAC
XR_949471.3:n.3760+45_3760+46insAC
XR_949472.3:n.3760+45_3760+46insAC
NM_000553.6:c.3459+45_3459+46insAC MANE Select	NP_000544.2:n.3459+45_3459+46insAC