Canonical Allele Identifier: CA2716980264

Gene: WRN

Linked Data

• dbSNP Id: rs2130316094

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31119132C>T , CM000670.2:g.31119132C>T	GRCh38
NC_000008.10:g.30976648C>T , CM000670.1:g.30976648C>T	GRCh37
NC_000008.9:g.31096190C>T	NCBI36
NG_008870.1:g.90871C>T , LRG_524:g.90871C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000298139.7:c.2449-1111C>T MANE Select	ENSP00000298139.5:n.2449-1111C>T
ENST00000650667.1:c.*2063-1111C>T	ENSP00000498593.1:n.*2063-1111C>T
ENST00000298139.5:c.2449-1111C>T	ENSP00000298139.5:n.2449-1111C>T
ENST00000521620.5:n.1082-1111C>T
NM_000553.4:c.2449-1111C>T , LRG_524t1:c.2449-1111C>T	NP_000544.2:n.2449-1111C>T
XM_011544639.1:c.2368-1111C>T	XP_011542941.1:n.2368-1111C>T
XM_011544640.1:c.850-1111C>T	XP_011542942.1:n.850-1111C>T
XR_949470.1:n.2722-1111C>T
XR_949471.1:n.2722-1111C>T
XR_949472.1:n.2722-1111C>T
NM_000553.5:c.2449-1111C>T	NP_000544.2:n.2449-1111C>T
XM_011544639.3:c.2368-1111C>T	XP_011542941.1:n.2368-1111C>T
XM_024447265.1:c.2239-1111C>T	XP_024303033.1:n.2239-1111C>T
XR_949470.3:n.2750-1111C>T
XR_949471.3:n.2750-1111C>T
XR_949472.3:n.2750-1111C>T
NM_000553.6:c.2449-1111C>T MANE Select	NP_000544.2:n.2449-1111C>T