Canonical Allele Identifier: CA2686840623

Gene: WRN

Linked Data

• gnomAD v4: 8-31173177-AGGAGTAGTATTTT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31173180_31173192del , CM000670.2:g.31173180_31173192del	GRCh38
NC_000008.10:g.31030696_31030708del , CM000670.1:g.31030696_31030708del	GRCh37
NC_000008.9:g.31150238_31150250del	NCBI36
NG_008870.1:g.144919_144931del , LRG_524:g.144919_144931del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298139.7:c.*78_*90del MANE Select	ENSP00000298139.5:n.*78_*90del
ENST00000650667.1:c.*3991_*4003del	ENSP00000498593.1:n.*3991_*4003del
ENST00000651946.1:n.601_613del
ENST00000298139.5:c.*78_*90del	ENSP00000298139.5:n.*78_*90del
ENST00000521620.5:n.3010_3022del
NM_000553.4:c.*78_*90del , LRG_524t1:c.*78_*90del	NP_000544.2:n.*78_*90del
XM_011544639.1:c.*78_*90del	XP_011542941.1:n.*78_*90del
XM_011544640.1:c.*78_*90del	XP_011542942.1:n.*78_*90del
XR_949643.1:n.88-1872_88-1860del
XR_949644.1:n.88-1872_88-1860del
XR_949645.1:n.88-1872_88-1860del
XR_949646.1:n.88-1872_88-1860del
XR_949647.1:n.701-1872_701-1860del
XR_949648.1:n.603-1872_603-1860del
NM_000553.5:c.*78_*90del	NP_000544.2:n.*78_*90del
XM_011544639.3:c.*78_*90del	XP_011542941.1:n.*78_*90del
XM_024447265.1:c.*78_*90del	XP_024303033.1:n.*78_*90del
NM_000553.6:c.*78_*90del MANE Select	NP_000544.2:n.*78_*90del