Canonical Allele Identifier: CA370912341

Gene: WRN

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31111614G>C , CM000670.2:g.31111614G>C	GRCh38
NC_000008.10:g.30969130G>C , CM000670.1:g.30969130G>C	GRCh37
NC_000008.9:g.31088672G>C	NCBI36
NG_008870.1:g.83353G>C , LRG_524:g.83353G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298139.7:c.2089-1G>C MANE Select	ENSP00000298139.5:n.2089-1G>C
ENST00000650667.1:c.*1703-1G>C	ENSP00000498593.1:n.*1703-1G>C
ENST00000298139.5:c.2089-1G>C	ENSP00000298139.5:n.2089-1G>C
ENST00000521620.5:n.722-1G>C
NM_000553.4:c.2089-1G>C , LRG_524t1:c.2089-1G>C	NP_000544.2:n.2089-1G>C
XM_011544639.1:c.2008-1G>C	XP_011542941.1:n.2008-1G>C
XM_011544640.1:c.490-1G>C	XP_011542942.1:n.490-1G>C
XR_949470.1:n.2362-1G>C
XR_949471.1:n.2362-1G>C
XR_949472.1:n.2362-1G>C
NM_000553.5:c.2089-1G>C	NP_000544.2:n.2089-1G>C
XM_011544639.3:c.2008-1G>C	XP_011542941.1:n.2008-1G>C
XM_024447265.1:c.1879-1G>C	XP_024303033.1:n.1879-1G>C
XR_949470.3:n.2390-1G>C
XR_949471.3:n.2390-1G>C
XR_949472.3:n.2390-1G>C
NM_000553.6:c.2089-1G>C MANE Select	NP_000544.2:n.2089-1G>C