Canonical Allele Identifier: CA370916382

Gene: WRN

Linked Data

• MyVariant Identifiers: chr8:g.30924680T>G (hg19) ; chr8:g.31067164T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31067164T>G , CM000670.2:g.31067164T>G	GRCh38
NC_000008.10:g.30924680T>G , CM000670.1:g.30924680T>G	GRCh37
NC_000008.9:g.31044222T>G	NCBI36
NG_008870.1:g.38903T>G , LRG_524:g.38903T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298139.7:c.636T>G MANE Select	ENSP00000298139.5:p.Tyr212Ter
ENST00000650667.1:c.*250T>G	ENSP00000498593.1:n.*250T>G
ENST00000298139.5:c.636T>G	ENSP00000298139.5:p.Tyr212Ter
NM_000553.4:c.636T>G , LRG_524t1:c.636T>G	NP_000544.2:p.Tyr212Ter
XM_011544639.1:c.636T>G	XP_011542941.1:p.Tyr212Ter
XR_949470.1:n.909T>G
XR_949471.1:n.909T>G
XR_949472.1:n.909T>G
NM_000553.5:c.636T>G	NP_000544.2:p.Tyr212Ter
XM_011544639.3:c.636T>G	XP_011542941.1:p.Tyr212Ter
XM_024447265.1:c.426T>G	XP_024303033.1:p.Tyr142Ter
XR_949470.3:n.937T>G
XR_949471.3:n.937T>G
XR_949472.3:n.937T>G
NM_000553.6:c.636T>G MANE Select	NP_000544.2:p.Tyr212Ter