Canonical Allele Identifier: CA2716983721

Gene: WRN

Linked Data

• dbSNP Id: rs2130440275

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31147311C>G , CM000670.2:g.31147311C>G	GRCh38
NC_000008.10:g.31004827C>G , CM000670.1:g.31004827C>G	GRCh37
NC_000008.9:g.31124369C>G	NCBI36
NG_008870.1:g.119050C>G , LRG_524:g.119050C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298139.7:c.3460-53C>G MANE Select	ENSP00000298139.5:n.3460-53C>G
ENST00000650667.1:c.*3074-53C>G	ENSP00000498593.1:n.*3074-53C>G
ENST00000298139.5:c.3460-53C>G	ENSP00000298139.5:n.3460-53C>G
ENST00000521620.5:n.2093-53C>G
NM_000553.4:c.3460-53C>G , LRG_524t1:c.3460-53C>G	NP_000544.2:n.3460-53C>G
XM_011544639.1:c.3379-53C>G	XP_011542941.1:n.3379-53C>G
XM_011544640.1:c.1861-53C>G	XP_011542942.1:n.1861-53C>G
XR_949470.1:n.3733-53C>G
XR_949471.1:n.3733-53C>G
XR_949472.1:n.3733-53C>G
XR_949643.1:n.614+1197G>C
NM_000553.5:c.3460-53C>G	NP_000544.2:n.3460-53C>G
XM_011544639.3:c.3379-53C>G	XP_011542941.1:n.3379-53C>G
XM_024447265.1:c.3250-53C>G	XP_024303033.1:n.3250-53C>G
XR_949470.3:n.3761-53C>G
XR_949471.3:n.3761-53C>G
XR_949472.3:n.3761-53C>G
NM_000553.6:c.3460-53C>G MANE Select	NP_000544.2:n.3460-53C>G