Canonical Allele Identifier: CA2686840052

Gene: WRN

Linked Data

• dbSNP Id: rs2130469194
• gnomAD v4: 8-31154522-TTTAAC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31154525_31154529del , CM000670.2:g.31154525_31154529del	GRCh38
NC_000008.10:g.31012041_31012045del , CM000670.1:g.31012041_31012045del	GRCh37
NC_000008.9:g.31131583_31131587del	NCBI36
NG_008870.1:g.126264_126268del , LRG_524:g.126264_126268del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298139.7:c.3688-99_3688-95del MANE Select	ENSP00000298139.5:n.3688-99_3688-95del
ENST00000650667.1:c.*3302-99_*3302-95del	ENSP00000498593.1:n.*3302-99_*3302-95del
ENST00000298139.5:c.3688-99_3688-95del	ENSP00000298139.5:n.3688-99_3688-95del
ENST00000521620.5:n.2321-99_2321-95del
NM_000553.4:c.3688-99_3688-95del , LRG_524t1:c.3688-99_3688-95del	NP_000544.2:n.3688-99_3688-95del
XM_011544639.1:c.3607-99_3607-95del	XP_011542941.1:n.3607-99_3607-95del
XM_011544640.1:c.2089-99_2089-95del	XP_011542942.1:n.2089-99_2089-95del
XR_949470.1:n.3961-99_3961-95del
XR_949471.1:n.3961-99_3961-95del
XR_949472.1:n.3961-99_3961-95del
XR_949643.1:n.457-5862_457-5858del
XR_949644.1:n.381-5862_381-5858del
XR_949647.1:n.1070-5862_1070-5858del
XR_949648.1:n.972-5862_972-5858del
NM_000553.5:c.3688-99_3688-95del	NP_000544.2:n.3688-99_3688-95del
XM_011544639.3:c.3607-99_3607-95del	XP_011542941.1:n.3607-99_3607-95del
XM_024447265.1:c.3478-99_3478-95del	XP_024303033.1:n.3478-99_3478-95del
XR_949470.3:n.3989-99_3989-95del
XR_949471.3:n.3989-99_3989-95del
XR_949472.3:n.3989-99_3989-95del
NM_000553.6:c.3688-99_3688-95del MANE Select	NP_000544.2:n.3688-99_3688-95del