Canonical Allele Identifier: CA10630912

Gene: WRN

Linked Data

• ClinVar Variation Id: 362788
• ClinVar RCV Id: RCV000371648
• dbSNP Id: rs886062883
• MyVariant Identifiers: chr8:g.30891332T>A (hg19) ; chr8:g.31033816T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31033816T>A , CM000670.2:g.31033816T>A	GRCh38
NC_000008.10:g.30891332T>A , CM000670.1:g.30891332T>A	GRCh37
NC_000008.9:g.31010874T>A	NCBI36
NG_008870.1:g.5555T>A , LRG_524:g.5555T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298139.7:c.-234T>A MANE Select	ENSP00000298139.5:n.-234T>A
ENST00000650667.1:c.-234T>A	ENSP00000498593.1:n.-234T>A
ENST00000298139.5:c.-234T>A	ENSP00000298139.5:n.-234T>A
NM_000553.4:c.-234T>A , LRG_524t1:c.-234T>A	NP_000544.2:n.-234T>A
XM_011544639.1:c.-234T>A	XP_011542941.1:n.-234T>A
XR_949470.1:n.40T>A
XR_949471.1:n.40T>A
XR_949472.1:n.40T>A
NM_000553.5:c.-234T>A	NP_000544.2:n.-234T>A
XM_011544639.3:c.-234T>A	XP_011542941.1:n.-234T>A
XM_024447265.1:c.-568T>A	XP_024303033.1:n.-568T>A
XR_949470.3:n.68T>A
XR_949471.3:n.68T>A
XR_949472.3:n.68T>A
NM_000553.6:c.-234T>A MANE Select	NP_000544.2:n.-234T>A