Canonical Allele Identifier: CA2740094999

Gene: WRN

Linked Data

• ClinVar Variation Id: 3004969
• ClinVar RCV Id: RCV003861072

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31067196G>A , CM000670.2:g.31067196G>A	GRCh38
NC_000008.10:g.30924712G>A , CM000670.1:g.30924712G>A	GRCh37
NC_000008.9:g.31044254G>A	NCBI36
NG_008870.1:g.38935G>A , LRG_524:g.38935G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298139.7:c.654+14G>A MANE Select	ENSP00000298139.5:n.654+14G>A
ENST00000650667.1:c.*268+14G>A	ENSP00000498593.1:n.*268+14G>A
ENST00000298139.5:c.654+14G>A	ENSP00000298139.5:n.654+14G>A
NM_000553.4:c.654+14G>A , LRG_524t1:c.654+14G>A	NP_000544.2:n.654+14G>A
XM_011544639.1:c.654+14G>A	XP_011542941.1:n.654+14G>A
XR_949470.1:n.927+14G>A
XR_949471.1:n.927+14G>A
XR_949472.1:n.927+14G>A
NM_000553.5:c.654+14G>A	NP_000544.2:n.654+14G>A
XM_011544639.3:c.654+14G>A	XP_011542941.1:n.654+14G>A
XM_024447265.1:c.444+14G>A	XP_024303033.1:n.444+14G>A
XR_949470.3:n.955+14G>A
XR_949471.3:n.955+14G>A
XR_949472.3:n.955+14G>A
NM_000553.6:c.654+14G>A MANE Select	NP_000544.2:n.654+14G>A