Canonical Allele Identifier: CA370916403

Gene: WRN

Linked Data

• dbSNP Id: rs778470570
• MyVariant Identifiers: chr8:g.30924685C>T (hg19) ; chr8:g.31067169C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31067169C>T , CM000670.2:g.31067169C>T	GRCh38
NC_000008.10:g.30924685C>T , CM000670.1:g.30924685C>T	GRCh37
NC_000008.9:g.31044227C>T	NCBI36
NG_008870.1:g.38908C>T , LRG_524:g.38908C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298139.7:c.641C>T MANE Select	ENSP00000298139.5:p.Ala214Val
ENST00000650667.1:c.*255C>T	ENSP00000498593.1:n.*255C>T
ENST00000298139.5:c.641C>T	ENSP00000298139.5:p.Ala214Val
NM_000553.4:c.641C>T , LRG_524t1:c.641C>T	NP_000544.2:p.Ala214Val
XM_011544639.1:c.641C>T	XP_011542941.1:p.Ala214Val
XR_949470.1:n.914C>T
XR_949471.1:n.914C>T
XR_949472.1:n.914C>T
NM_000553.5:c.641C>T	NP_000544.2:p.Ala214Val
XM_011544639.3:c.641C>T	XP_011542941.1:p.Ala214Val
XM_024447265.1:c.431C>T	XP_024303033.1:p.Ala144Val
XR_949470.3:n.942C>T
XR_949471.3:n.942C>T
XR_949472.3:n.942C>T
NM_000553.6:c.641C>T MANE Select	NP_000544.2:p.Ala214Val