Canonical Allele Identifier: CA370915924

Gene: WRN

Linked Data

• MyVariant Identifiers: chr8:g.30924571G>C (hg19) ; chr8:g.31067055G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31067055G>C , CM000670.2:g.31067055G>C	GRCh38
NC_000008.10:g.30924571G>C , CM000670.1:g.30924571G>C	GRCh37
NC_000008.9:g.31044113G>C	NCBI36
NG_008870.1:g.38794G>C , LRG_524:g.38794G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000298139.7:c.527G>C MANE Select	ENSP00000298139.5:p.Ser176Thr
ENST00000650667.1:c.*141G>C	ENSP00000498593.1:n.*141G>C
ENST00000298139.5:c.527G>C	ENSP00000298139.5:p.Ser176Thr
NM_000553.4:c.527G>C , LRG_524t1:c.527G>C	NP_000544.2:p.Ser176Thr
XM_011544639.1:c.527G>C	XP_011542941.1:p.Ser176Thr
XR_949470.1:n.800G>C
XR_949471.1:n.800G>C
XR_949472.1:n.800G>C
NM_000553.5:c.527G>C	NP_000544.2:p.Ser176Thr
XM_011544639.3:c.527G>C	XP_011542941.1:p.Ser176Thr
XM_024447265.1:c.317G>C	XP_024303033.1:p.Ser106Thr
XR_949470.3:n.828G>C
XR_949471.3:n.828G>C
XR_949472.3:n.828G>C
NM_000553.6:c.527G>C MANE Select	NP_000544.2:p.Ser176Thr