Canonical Allele Identifier: CA370911801

Gene: WRN

Linked Data

• ClinVar Variation Id: 2632224
• ClinVar RCV Id: RCV003406066
• gnomAD v4: 8-31173062-A-G
• MyVariant Identifiers: chr8:g.31030578A>G (hg19) ; chr8:g.31173062A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31173062A>G , CM000670.2:g.31173062A>G	GRCh38
NC_000008.10:g.31030578A>G , CM000670.1:g.31030578A>G	GRCh37
NC_000008.9:g.31150120A>G	NCBI36
NG_008870.1:g.144801A>G , LRG_524:g.144801A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298139.7:c.4259A>G MANE Select	ENSP00000298139.5:p.Lys1420Arg
ENST00000650667.1:c.*3873A>G	ENSP00000498593.1:n.*3873A>G
ENST00000651946.1:n.483A>G
ENST00000298139.5:c.4259A>G	ENSP00000298139.5:p.Lys1420Arg
ENST00000521620.5:n.2892A>G
NM_000553.4:c.4259A>G , LRG_524t1:c.4259A>G	NP_000544.2:p.Lys1420Arg
XM_011544639.1:c.4178A>G	XP_011542941.1:p.Lys1393Arg
XM_011544640.1:c.2660A>G	XP_011542942.1:p.Lys887Arg
XR_949643.1:n.88-1744T>C
XR_949644.1:n.88-1744T>C
XR_949645.1:n.88-1744T>C
XR_949646.1:n.88-1744T>C
XR_949647.1:n.701-1744T>C
XR_949648.1:n.603-1744T>C
NM_000553.5:c.4259A>G	NP_000544.2:p.Lys1420Arg
XM_011544639.3:c.4178A>G	XP_011542941.1:p.Lys1393Arg
XM_024447265.1:c.4049A>G	XP_024303033.1:p.Lys1350Arg
NM_000553.6:c.4259A>G MANE Select	NP_000544.2:p.Lys1420Arg