Canonical Allele Identifier: CA2497474567

Gene: WRN

Linked Data

• ClinVar Variation Id: 2741881
• ClinVar RCV Id: RCV003506722
• dbSNP Id: rs1812743061
• gnomAD v4: 8-31067185-A-ACGT

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31067186_31067188dup , CM000670.2:g.31067186_31067188dup	GRCh38
NC_000008.10:g.30924702_30924704dup , CM000670.1:g.30924702_30924704dup	GRCh37
NC_000008.9:g.31044244_31044246dup	NCBI36
NG_008870.1:g.38925_38927dup , LRG_524:g.38925_38927dup

Transcript Alleles

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