Canonical Allele Identifier: CA580995266

Gene: WRN

Linked Data

• dbSNP Id: rs1385115258
• gnomAD v2: 8-30924482-T-TG
• gnomAD v3: 8-31066966-T-TG
• gnomAD v4: 8-31066966-T-TG
• MyVariant Identifiers: chr8:g.30924482_30924483insG (hg19) ; chr8:g.31066966_31066967insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31066967dup , CM000670.2:g.31066967dup	GRCh38
NC_000008.10:g.30924483dup , CM000670.1:g.30924483dup	GRCh37
NC_000008.9:g.31044025dup	NCBI36
NG_008870.1:g.38706dup , LRG_524:g.38706dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298139.7:c.505-66dup MANE Select	ENSP00000298139.5:n.505-66dup
ENST00000650667.1:c.*119-66dup	ENSP00000498593.1:n.*119-66dup
ENST00000298139.5:c.505-66dup	ENSP00000298139.5:n.505-66dup
NM_000553.4:c.505-66dup , LRG_524t1:c.505-66dup	NP_000544.2:n.505-66dup
XM_011544639.1:c.505-66dup	XP_011542941.1:n.505-66dup
XR_949470.1:n.778-66dup
XR_949471.1:n.778-66dup
XR_949472.1:n.778-66dup
NM_000553.5:c.505-66dup	NP_000544.2:n.505-66dup
XM_011544639.3:c.505-66dup	XP_011542941.1:n.505-66dup
XM_024447265.1:c.295-66dup	XP_024303033.1:n.295-66dup
XR_949470.3:n.806-66dup
XR_949471.3:n.806-66dup
XR_949472.3:n.806-66dup
NM_000553.6:c.505-66dup MANE Select	NP_000544.2:n.505-66dup