Canonical Allele Identifier: CA370911561

Gene: WRN

Linked Data

• MyVariant Identifiers: chr8:g.31030525G>C (hg19) ; chr8:g.31173009G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31173009G>C , CM000670.2:g.31173009G>C	GRCh38
NC_000008.10:g.31030525G>C , CM000670.1:g.31030525G>C	GRCh37
NC_000008.9:g.31150067G>C	NCBI36
NG_008870.1:g.144748G>C , LRG_524:g.144748G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298139.7:c.4206G>C MANE Select	ENSP00000298139.5:p.Glu1402Asp
ENST00000650667.1:c.*3820G>C	ENSP00000498593.1:n.*3820G>C
ENST00000651946.1:n.430G>C
ENST00000298139.5:c.4206G>C	ENSP00000298139.5:p.Glu1402Asp
ENST00000521620.5:n.2839G>C
NM_000553.4:c.4206G>C , LRG_524t1:c.4206G>C	NP_000544.2:p.Glu1402Asp
XM_011544639.1:c.4125G>C	XP_011542941.1:p.Glu1375Asp
XM_011544640.1:c.2607G>C	XP_011542942.1:p.Glu869Asp
XR_949643.1:n.88-1691C>G
XR_949644.1:n.88-1691C>G
XR_949645.1:n.88-1691C>G
XR_949646.1:n.88-1691C>G
XR_949647.1:n.701-1691C>G
XR_949648.1:n.603-1691C>G
NM_000553.5:c.4206G>C	NP_000544.2:p.Glu1402Asp
XM_011544639.3:c.4125G>C	XP_011542941.1:p.Glu1375Asp
XM_024447265.1:c.3996G>C	XP_024303033.1:p.Glu1332Asp
NM_000553.6:c.4206G>C MANE Select	NP_000544.2:p.Glu1402Asp