Canonical Allele Identifier: CA2686835125

Gene: WRN

Linked Data

• gnomAD v4: 8-31067265-AGTG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31067267_31067269del , CM000670.2:g.31067267_31067269del	GRCh38
NC_000008.10:g.30924783_30924785del , CM000670.1:g.30924783_30924785del	GRCh37
NC_000008.9:g.31044325_31044327del	NCBI36
NG_008870.1:g.39006_39008del , LRG_524:g.39006_39008del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298139.7:c.654+85_654+87del MANE Select	ENSP00000298139.5:n.654+85_654+87del
ENST00000650667.1:c.*268+85_*268+87del	ENSP00000498593.1:n.*268+85_*268+87del
ENST00000298139.5:c.654+85_654+87del	ENSP00000298139.5:n.654+85_654+87del
NM_000553.4:c.654+85_654+87del , LRG_524t1:c.654+85_654+87del	NP_000544.2:n.654+85_654+87del
XM_011544639.1:c.654+85_654+87del	XP_011542941.1:n.654+85_654+87del
XR_949470.1:n.927+85_927+87del
XR_949471.1:n.927+85_927+87del
XR_949472.1:n.927+85_927+87del
NM_000553.5:c.654+85_654+87del	NP_000544.2:n.654+85_654+87del
XM_011544639.3:c.654+85_654+87del	XP_011542941.1:n.654+85_654+87del
XM_024447265.1:c.444+85_444+87del	XP_024303033.1:n.444+85_444+87del
XR_949470.3:n.955+85_955+87del
XR_949471.3:n.955+85_955+87del
XR_949472.3:n.955+85_955+87del
NM_000553.6:c.654+85_654+87del MANE Select	NP_000544.2:n.654+85_654+87del