Canonical Allele Identifier: CA370911659
Gene: WRN HGNC NCBI

Linked Data

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