Canonical Allele Identifier: CA370925821
Gene: WRN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.31147412A>T , CM000670.2:g.31147412A>T GRCh38
NC_000008.10:g.31004928A>T , CM000670.1:g.31004928A>T GRCh37
NC_000008.9:g.31124470A>T NCBI36
NG_008870.1:g.119151A>T , LRG_524:g.119151A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000298139.7:c.3508A>T MANE Select ENSP00000298139.5:p.Lys1170Ter
ENST00000650667.1:c.*3122A>T ENSP00000498593.1:n.*3122A>T
ENST00000298139.5:c.3508A>T ENSP00000298139.5:p.Lys1170Ter
ENST00000521620.5:n.2141A>T
NM_000553.4:c.3508A>T , LRG_524t1:c.3508A>T NP_000544.2:p.Lys1170Ter
XM_011544639.1:c.3427A>T XP_011542941.1:p.Lys1143Ter
XM_011544640.1:c.1909A>T XP_011542942.1:p.Lys637Ter
XR_949470.1:n.3781A>T
XR_949471.1:n.3781A>T
XR_949472.1:n.3781A>T
XR_949643.1:n.614+1096T>A
NM_000553.5:c.3508A>T NP_000544.2:p.Lys1170Ter
XM_011544639.3:c.3427A>T XP_011542941.1:p.Lys1143Ter
XM_024447265.1:c.3298A>T XP_024303033.1:p.Lys1100Ter
XR_949470.3:n.3809A>T
XR_949471.3:n.3809A>T
XR_949472.3:n.3809A>T
NM_000553.6:c.3508A>T MANE Select NP_000544.2:p.Lys1170Ter