Canonical Allele Identifier: CA580995525

Gene: WRN

Linked Data

• gnomAD v2: 8-30925867-A-AC
• MyVariant Identifiers: chr8:g.30925867_30925868insC (hg19) ; chr8:g.31068351_31068352insC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31068351_31068352insC , CM000670.2:g.31068351_31068352insC	GRCh38
NC_000008.10:g.30925867_30925868insC , CM000670.1:g.30925867_30925868insC	GRCh37
NC_000008.9:g.31045409_31045410insC	NCBI36
NG_008870.1:g.40090_40091insC , LRG_524:g.40090_40091insC

Transcript Alleles

HGVS	Amino-acid change
ENST00000298139.7:c.724+24_724+25insC MANE Select	ENSP00000298139.5:n.724+24_724+25insC
ENST00000650667.1:c.*338+24_*338+25insC	ENSP00000498593.1:n.*338+24_*338+25insC
ENST00000651642.1:c.19+24_19+25insC	ENSP00000498779.1:n.19+24_19+25insC
ENST00000298139.5:c.724+24_724+25insC	ENSP00000298139.5:n.724+24_724+25insC
NM_000553.4:c.724+24_724+25insC , LRG_524t1:c.724+24_724+25insC	NP_000544.2:n.724+24_724+25insC
XM_011544639.1:c.724+24_724+25insC	XP_011542941.1:n.724+24_724+25insC
XR_949470.1:n.997+24_997+25insC
XR_949471.1:n.997+24_997+25insC
XR_949472.1:n.997+24_997+25insC
NM_000553.5:c.724+24_724+25insC	NP_000544.2:n.724+24_724+25insC
XM_011544639.3:c.724+24_724+25insC	XP_011542941.1:n.724+24_724+25insC
XM_024447265.1:c.514+24_514+25insC	XP_024303033.1:n.514+24_514+25insC
XR_949470.3:n.1025+24_1025+25insC
XR_949471.3:n.1025+24_1025+25insC
XR_949472.3:n.1025+24_1025+25insC
NM_000553.6:c.724+24_724+25insC MANE Select	NP_000544.2:n.724+24_724+25insC