Canonical Allele Identifier: CA580995518

Gene: WRN

Linked Data

• dbSNP Id: rs1212673267
• gnomAD v2: 8-30925856-C-CA
• MyVariant Identifiers: chr8:g.30925856_30925857insA (hg19) ; chr8:g.31068340_31068341insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31068340_31068341insA , CM000670.2:g.31068340_31068341insA	GRCh38
NC_000008.10:g.30925856_30925857insA , CM000670.1:g.30925856_30925857insA	GRCh37
NC_000008.9:g.31045398_31045399insA	NCBI36
NG_008870.1:g.40079_40080insA , LRG_524:g.40079_40080insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298139.7:c.724+13_724+14insA MANE Select	ENSP00000298139.5:n.724+13_724+14insA
ENST00000650667.1:c.*338+13_*338+14insA	ENSP00000498593.1:n.*338+13_*338+14insA
ENST00000651642.1:c.19+13_19+14insA	ENSP00000498779.1:n.19+13_19+14insA
ENST00000298139.5:c.724+13_724+14insA	ENSP00000298139.5:n.724+13_724+14insA
NM_000553.4:c.724+13_724+14insA , LRG_524t1:c.724+13_724+14insA	NP_000544.2:n.724+13_724+14insA
XM_011544639.1:c.724+13_724+14insA	XP_011542941.1:n.724+13_724+14insA
XR_949470.1:n.997+13_997+14insA
XR_949471.1:n.997+13_997+14insA
XR_949472.1:n.997+13_997+14insA
NM_000553.5:c.724+13_724+14insA	NP_000544.2:n.724+13_724+14insA
XM_011544639.3:c.724+13_724+14insA	XP_011542941.1:n.724+13_724+14insA
XM_024447265.1:c.514+13_514+14insA	XP_024303033.1:n.514+13_514+14insA
XR_949470.3:n.1025+13_1025+14insA
XR_949471.3:n.1025+13_1025+14insA
XR_949472.3:n.1025+13_1025+14insA
NM_000553.6:c.724+13_724+14insA MANE Select	NP_000544.2:n.724+13_724+14insA