Canonical Allele Identifier: CA850720902

Gene: WRN

Linked Data

• dbSNP Id: rs1408271660
• MyVariant Identifiers: chr8:g.30924320A>T (hg19) ; chr8:g.31066804A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31066804A>T , CM000670.2:g.31066804A>T	GRCh38
NC_000008.10:g.30924320A>T , CM000670.1:g.30924320A>T	GRCh37
NC_000008.9:g.31043862A>T	NCBI36
NG_008870.1:g.38543A>T , LRG_524:g.38543A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298139.7:c.505-229A>T MANE Select	ENSP00000298139.5:n.505-229A>T
ENST00000650667.1:c.*119-229A>T	ENSP00000498593.1:n.*119-229A>T
ENST00000298139.5:c.505-229A>T	ENSP00000298139.5:n.505-229A>T
NM_000553.4:c.505-229A>T , LRG_524t1:c.505-229A>T	NP_000544.2:n.505-229A>T
XM_011544639.1:c.505-229A>T	XP_011542941.1:n.505-229A>T
XR_949470.1:n.778-229A>T
XR_949471.1:n.778-229A>T
XR_949472.1:n.778-229A>T
NM_000553.5:c.505-229A>T	NP_000544.2:n.505-229A>T
XM_011544639.3:c.505-229A>T	XP_011542941.1:n.505-229A>T
XM_024447265.1:c.295-229A>T	XP_024303033.1:n.295-229A>T
XR_949470.3:n.806-229A>T
XR_949471.3:n.806-229A>T
XR_949472.3:n.806-229A>T
NM_000553.6:c.505-229A>T MANE Select	NP_000544.2:n.505-229A>T