Canonical Allele Identifier: CA4704141

Gene: WRN

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31068327G>C , CM000670.2:g.31068327G>C	GRCh38
NC_000008.10:g.30925843G>C , CM000670.1:g.30925843G>C	GRCh37
NC_000008.9:g.31045385G>C	NCBI36
NG_008870.1:g.40066G>C , LRG_524:g.40066G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_000553.6:c.724G>C MANE Select	NP_000544.2:p.Glu242Gln
ENST00000298139.7:c.724G>C MANE Select	ENSP00000298139.5:p.Glu242Gln
NM_000553.4:c.724G>C , LRG_524t1:c.724G>C	NP_000544.2:p.Glu242Gln
NM_000553.5:c.724G>C	NP_000544.2:p.Glu242Gln
ENST00000298139.5:c.724G>C	ENSP00000298139.5:p.Glu242Gln
ENST00000650667.1:c.*338G>C	ENSP00000498593.1:n.*338G>C
ENST00000651642.1:c.19G>C	ENSP00000498779.1:p.Glu7Gln
XM_011544639.1:c.724G>C	XP_011542941.1:p.Glu242Gln
XM_011544639.3:c.724G>C	XP_011542941.1:p.Glu242Gln
XM_024447265.1:c.514G>C	XP_024303033.1:p.Glu172Gln
XR_949470.1:n.997G>C
XR_949470.3:n.1025G>C
XR_949471.1:n.997G>C
XR_949471.3:n.1025G>C
XR_949472.1:n.997G>C
XR_949472.3:n.1025G>C