Canonical Allele Identifier: CA370916245
Gene: WRN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.31067132A>T , CM000670.2:g.31067132A>T GRCh38
NC_000008.10:g.30924648A>T , CM000670.1:g.30924648A>T GRCh37
NC_000008.9:g.31044190A>T NCBI36
NG_008870.1:g.38871A>T , LRG_524:g.38871A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000298139.7:c.604A>T MANE Select ENSP00000298139.5:p.Lys202Ter
ENST00000650667.1:c.*218A>T ENSP00000498593.1:n.*218A>T
ENST00000298139.5:c.604A>T ENSP00000298139.5:p.Lys202Ter
NM_000553.4:c.604A>T , LRG_524t1:c.604A>T NP_000544.2:p.Lys202Ter
XM_011544639.1:c.604A>T XP_011542941.1:p.Lys202Ter
XR_949470.1:n.877A>T
XR_949471.1:n.877A>T
XR_949472.1:n.877A>T
NM_000553.5:c.604A>T NP_000544.2:p.Lys202Ter
XM_011544639.3:c.604A>T XP_011542941.1:p.Lys202Ter
XM_024447265.1:c.394A>T XP_024303033.1:p.Lys132Ter
XR_949470.3:n.905A>T
XR_949471.3:n.905A>T
XR_949472.3:n.905A>T
NM_000553.6:c.604A>T MANE Select NP_000544.2:p.Lys202Ter