Canonical Allele Identifier: CA370916081

Gene: WRN

Linked Data

• MyVariant Identifiers: chr8:g.30924612C>A (hg19) ; chr8:g.31067096C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31067096C>A , CM000670.2:g.31067096C>A	GRCh38
NC_000008.10:g.30924612C>A , CM000670.1:g.30924612C>A	GRCh37
NC_000008.9:g.31044154C>A	NCBI36
NG_008870.1:g.38835C>A , LRG_524:g.38835C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298139.7:c.568C>A MANE Select	ENSP00000298139.5:p.Leu190Met
ENST00000650667.1:c.*182C>A	ENSP00000498593.1:n.*182C>A
ENST00000298139.5:c.568C>A	ENSP00000298139.5:p.Leu190Met
NM_000553.4:c.568C>A , LRG_524t1:c.568C>A	NP_000544.2:p.Leu190Met
XM_011544639.1:c.568C>A	XP_011542941.1:p.Leu190Met
XR_949470.1:n.841C>A
XR_949471.1:n.841C>A
XR_949472.1:n.841C>A
NM_000553.5:c.568C>A	NP_000544.2:p.Leu190Met
XM_011544639.3:c.568C>A	XP_011542941.1:p.Leu190Met
XM_024447265.1:c.358C>A	XP_024303033.1:p.Leu120Met
XR_949470.3:n.869C>A
XR_949471.3:n.869C>A
XR_949472.3:n.869C>A
NM_000553.6:c.568C>A MANE Select	NP_000544.2:p.Leu190Met