Canonical Allele Identifier: CA2579138130

Gene: WRN

Linked Data

• gnomAD v4: 8-31154564-ATATAT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31154566_31154570del , CM000670.2:g.31154566_31154570del	GRCh38
NC_000008.10:g.31012082_31012086del , CM000670.1:g.31012082_31012086del	GRCh37
NC_000008.9:g.31131624_31131628del	NCBI36
NG_008870.1:g.126305_126309del , LRG_524:g.126305_126309del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298139.7:c.3688-58_3688-54del MANE Select	ENSP00000298139.5:n.3688-58_3688-54del
ENST00000650667.1:c.*3302-58_*3302-54del	ENSP00000498593.1:n.*3302-58_*3302-54del
ENST00000298139.5:c.3688-58_3688-54del	ENSP00000298139.5:n.3688-58_3688-54del
ENST00000521620.5:n.2321-58_2321-54del
NM_000553.4:c.3688-58_3688-54del , LRG_524t1:c.3688-58_3688-54del	NP_000544.2:n.3688-58_3688-54del
XM_011544639.1:c.3607-58_3607-54del	XP_011542941.1:n.3607-58_3607-54del
XM_011544640.1:c.2089-58_2089-54del	XP_011542942.1:n.2089-58_2089-54del
XR_949470.1:n.3961-58_3961-54del
XR_949471.1:n.3961-58_3961-54del
XR_949472.1:n.3961-58_3961-54del
XR_949643.1:n.457-5904_457-5900del
XR_949644.1:n.381-5904_381-5900del
XR_949647.1:n.1070-5904_1070-5900del
XR_949648.1:n.972-5904_972-5900del
NM_000553.5:c.3688-58_3688-54del	NP_000544.2:n.3688-58_3688-54del
XM_011544639.3:c.3607-58_3607-54del	XP_011542941.1:n.3607-58_3607-54del
XM_024447265.1:c.3478-58_3478-54del	XP_024303033.1:n.3478-58_3478-54del
XR_949470.3:n.3989-58_3989-54del
XR_949471.3:n.3989-58_3989-54del
XR_949472.3:n.3989-58_3989-54del
NM_000553.6:c.3688-58_3688-54del MANE Select	NP_000544.2:n.3688-58_3688-54del