Canonical Allele Identifier: CA370911659

Gene: WRN

Linked Data

• MyVariant Identifiers: chr8:g.31030549G>C (hg19) ; chr8:g.31173033G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31173033G>C , CM000670.2:g.31173033G>C	GRCh38
NC_000008.10:g.31030549G>C , CM000670.1:g.31030549G>C	GRCh37
NC_000008.9:g.31150091G>C	NCBI36
NG_008870.1:g.144772G>C , LRG_524:g.144772G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298139.7:c.4230G>C MANE Select	ENSP00000298139.5:p.Trp1410Cys
ENST00000650667.1:c.*3844G>C	ENSP00000498593.1:n.*3844G>C
ENST00000651946.1:n.454G>C
ENST00000298139.5:c.4230G>C	ENSP00000298139.5:p.Trp1410Cys
ENST00000521620.5:n.2863G>C
NM_000553.4:c.4230G>C , LRG_524t1:c.4230G>C	NP_000544.2:p.Trp1410Cys
XM_011544639.1:c.4149G>C	XP_011542941.1:p.Trp1383Cys
XM_011544640.1:c.2631G>C	XP_011542942.1:p.Trp877Cys
XR_949643.1:n.88-1715C>G
XR_949644.1:n.88-1715C>G
XR_949645.1:n.88-1715C>G
XR_949646.1:n.88-1715C>G
XR_949647.1:n.701-1715C>G
XR_949648.1:n.603-1715C>G
NM_000553.5:c.4230G>C	NP_000544.2:p.Trp1410Cys
XM_011544639.3:c.4149G>C	XP_011542941.1:p.Trp1383Cys
XM_024447265.1:c.4020G>C	XP_024303033.1:p.Trp1340Cys
NM_000553.6:c.4230G>C MANE Select	NP_000544.2:p.Trp1410Cys