Canonical Allele Identifier: CA2686834160

Gene: WRN

Linked Data

• gnomAD v4: 8-31033844-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31033844A>G , CM000670.2:g.31033844A>G	GRCh38
NC_000008.10:g.30891360A>G , CM000670.1:g.30891360A>G	GRCh37
NC_000008.9:g.31010902A>G	NCBI36
NG_008870.1:g.5583A>G , LRG_524:g.5583A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298139.7:c.-206A>G MANE Select	ENSP00000298139.5:n.-206A>G
ENST00000650667.1:c.-206A>G	ENSP00000498593.1:n.-206A>G
ENST00000298139.5:c.-206A>G	ENSP00000298139.5:n.-206A>G
NM_000553.4:c.-206A>G , LRG_524t1:c.-206A>G	NP_000544.2:n.-206A>G
XM_011544639.1:c.-206A>G	XP_011542941.1:n.-206A>G
XR_949470.1:n.68A>G
XR_949471.1:n.68A>G
XR_949472.1:n.68A>G
NM_000553.5:c.-206A>G	NP_000544.2:n.-206A>G
XM_011544639.3:c.-206A>G	XP_011542941.1:n.-206A>G
XM_024447265.1:c.-540A>G	XP_024303033.1:n.-540A>G
XR_949470.3:n.96A>G
XR_949471.3:n.96A>G
XR_949472.3:n.96A>G
NM_000553.6:c.-206A>G MANE Select	NP_000544.2:n.-206A>G