Canonical Allele Identifier: CA2686838014

Gene: WRN

Linked Data

• gnomAD v4: 8-31120231-A-AT

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31120234dup , CM000670.2:g.31120234dup	GRCh38
NC_000008.10:g.30977750dup , CM000670.1:g.30977750dup	GRCh37
NC_000008.9:g.31097292dup	NCBI36
NG_008870.1:g.91973dup , LRG_524:g.91973dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298139.7:c.2449-9dup MANE Select	ENSP00000298139.5:n.2449-9dup
ENST00000650667.1:c.*2063-9dup	ENSP00000498593.1:n.*2063-9dup
ENST00000298139.5:c.2449-9dup	ENSP00000298139.5:n.2449-9dup
ENST00000520169.1:n.279dup
ENST00000521620.5:n.1082-9dup
NM_000553.4:c.2449-9dup , LRG_524t1:c.2449-9dup	NP_000544.2:n.2449-9dup
XM_011544639.1:c.2368-9dup	XP_011542941.1:n.2368-9dup
XM_011544640.1:c.850-9dup	XP_011542942.1:n.850-9dup
XR_949470.1:n.2722-9dup
XR_949471.1:n.2722-9dup
XR_949472.1:n.2722-9dup
NM_000553.5:c.2449-9dup	NP_000544.2:n.2449-9dup
XM_011544639.3:c.2368-9dup	XP_011542941.1:n.2368-9dup
XM_024447265.1:c.2239-9dup	XP_024303033.1:n.2239-9dup
XR_949470.3:n.2750-9dup
XR_949471.3:n.2750-9dup
XR_949472.3:n.2750-9dup
NM_000553.6:c.2449-9dup MANE Select	NP_000544.2:n.2449-9dup