Canonical Allele Identifier: CA580995537

Gene: WRN

Linked Data

• dbSNP Id: rs1563332063
• gnomAD v2: 8-30925877-A-AAC
• MyVariant Identifiers: chr8:g.30925877_30925878insAC (hg19) ; chr8:g.31068361_31068362insAC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31068361_31068362insAC , CM000670.2:g.31068361_31068362insAC	GRCh38
NC_000008.10:g.30925877_30925878insAC , CM000670.1:g.30925877_30925878insAC	GRCh37
NC_000008.9:g.31045419_31045420insAC	NCBI36
NG_008870.1:g.40100_40101insAC , LRG_524:g.40100_40101insAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298139.7:c.724+34_724+35insAC MANE Select	ENSP00000298139.5:n.724+34_724+35insAC
ENST00000650667.1:c.*338+34_*338+35insAC	ENSP00000498593.1:n.*338+34_*338+35insAC
ENST00000651642.1:c.19+34_19+35insAC	ENSP00000498779.1:n.19+34_19+35insAC
ENST00000298139.5:c.724+34_724+35insAC	ENSP00000298139.5:n.724+34_724+35insAC
NM_000553.4:c.724+34_724+35insAC , LRG_524t1:c.724+34_724+35insAC	NP_000544.2:n.724+34_724+35insAC
XM_011544639.1:c.724+34_724+35insAC	XP_011542941.1:n.724+34_724+35insAC
XR_949470.1:n.997+34_997+35insAC
XR_949471.1:n.997+34_997+35insAC
XR_949472.1:n.997+34_997+35insAC
NM_000553.5:c.724+34_724+35insAC	NP_000544.2:n.724+34_724+35insAC
XM_011544639.3:c.724+34_724+35insAC	XP_011542941.1:n.724+34_724+35insAC
XM_024447265.1:c.514+34_514+35insAC	XP_024303033.1:n.514+34_514+35insAC
XR_949470.3:n.1025+34_1025+35insAC
XR_949471.3:n.1025+34_1025+35insAC
XR_949472.3:n.1025+34_1025+35insAC
NM_000553.6:c.724+34_724+35insAC MANE Select	NP_000544.2:n.724+34_724+35insAC