Canonical Allele Identifier: CA2516336170

Gene: WRN

Linked Data

• gnomAD v4: 8-31173134-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31173134G>A , CM000670.2:g.31173134G>A	GRCh38
NC_000008.10:g.31030650G>A , CM000670.1:g.31030650G>A	GRCh37
NC_000008.9:g.31150192G>A	NCBI36
NG_008870.1:g.144873G>A , LRG_524:g.144873G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298139.7:c.*32G>A MANE Select	ENSP00000298139.5:n.*32G>A
ENST00000650667.1:c.*3945G>A	ENSP00000498593.1:n.*3945G>A
ENST00000651946.1:n.555G>A
ENST00000298139.5:c.*32G>A	ENSP00000298139.5:n.*32G>A
ENST00000521620.5:n.2964G>A
NM_000553.4:c.*32G>A , LRG_524t1:c.*32G>A	NP_000544.2:n.*32G>A
XM_011544639.1:c.*32G>A	XP_011542941.1:n.*32G>A
XM_011544640.1:c.*32G>A	XP_011542942.1:n.*32G>A
XR_949643.1:n.88-1816C>T
XR_949644.1:n.88-1816C>T
XR_949645.1:n.88-1816C>T
XR_949646.1:n.88-1816C>T
XR_949647.1:n.701-1816C>T
XR_949648.1:n.603-1816C>T
NM_000553.5:c.*32G>A	NP_000544.2:n.*32G>A
XM_011544639.3:c.*32G>A	XP_011542941.1:n.*32G>A
XM_024447265.1:c.*32G>A	XP_024303033.1:n.*32G>A
NM_000553.6:c.*32G>A MANE Select	NP_000544.2:n.*32G>A