Canonical Allele Identifier: CA370916237

Gene: WRN

Linked Data

• MyVariant Identifiers: chr8:g.30924646G>C (hg19) ; chr8:g.31067130G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31067130G>C , CM000670.2:g.31067130G>C	GRCh38
NC_000008.10:g.30924646G>C , CM000670.1:g.30924646G>C	GRCh37
NC_000008.9:g.31044188G>C	NCBI36
NG_008870.1:g.38869G>C , LRG_524:g.38869G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298139.7:c.602G>C MANE Select	ENSP00000298139.5:p.Ser201Thr
ENST00000650667.1:c.*216G>C	ENSP00000498593.1:n.*216G>C
ENST00000298139.5:c.602G>C	ENSP00000298139.5:p.Ser201Thr
NM_000553.4:c.602G>C , LRG_524t1:c.602G>C	NP_000544.2:p.Ser201Thr
XM_011544639.1:c.602G>C	XP_011542941.1:p.Ser201Thr
XR_949470.1:n.875G>C
XR_949471.1:n.875G>C
XR_949472.1:n.875G>C
NM_000553.5:c.602G>C	NP_000544.2:p.Ser201Thr
XM_011544639.3:c.602G>C	XP_011542941.1:p.Ser201Thr
XM_024447265.1:c.392G>C	XP_024303033.1:p.Ser131Thr
XR_949470.3:n.903G>C
XR_949471.3:n.903G>C
XR_949472.3:n.903G>C
NM_000553.6:c.602G>C MANE Select	NP_000544.2:p.Ser201Thr