Canonical Allele Identifier: CA2686835253

Gene: WRN

Linked Data

• gnomAD v4: 8-31068254-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31068254A>T , CM000670.2:g.31068254A>T	GRCh38
NC_000008.10:g.30925770A>T , CM000670.1:g.30925770A>T	GRCh37
NC_000008.9:g.31045312A>T	NCBI36
NG_008870.1:g.39993A>T , LRG_524:g.39993A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000298139.7:c.655-4A>T MANE Select	ENSP00000298139.5:n.655-4A>T
ENST00000650667.1:c.*269-4A>T	ENSP00000498593.1:n.*269-4A>T
ENST00000298139.5:c.655-4A>T	ENSP00000298139.5:n.655-4A>T
NM_000553.4:c.655-4A>T , LRG_524t1:c.655-4A>T	NP_000544.2:n.655-4A>T
XM_011544639.1:c.655-4A>T	XP_011542941.1:n.655-4A>T
XR_949470.1:n.928-4A>T
XR_949471.1:n.928-4A>T
XR_949472.1:n.928-4A>T
NM_000553.5:c.655-4A>T	NP_000544.2:n.655-4A>T
XM_011544639.3:c.655-4A>T	XP_011542941.1:n.655-4A>T
XM_024447265.1:c.445-4A>T	XP_024303033.1:n.445-4A>T
XR_949470.3:n.956-4A>T
XR_949471.3:n.956-4A>T
XR_949472.3:n.956-4A>T
NM_000553.6:c.655-4A>T MANE Select	NP_000544.2:n.655-4A>T