Canonical Allele Identifier: CA370911922
Gene: WRN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.31173089G>T , CM000670.2:g.31173089G>T GRCh38
NC_000008.10:g.31030605G>T , CM000670.1:g.31030605G>T GRCh37
NC_000008.9:g.31150147G>T NCBI36
NG_008870.1:g.144828G>T , LRG_524:g.144828G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000298139.7:c.4286G>T MANE Select ENSP00000298139.5:p.Gly1429Val
ENST00000650667.1:c.*3900G>T ENSP00000498593.1:n.*3900G>T
ENST00000651946.1:n.510G>T
ENST00000298139.5:c.4286G>T ENSP00000298139.5:p.Gly1429Val
ENST00000521620.5:n.2919G>T
NM_000553.4:c.4286G>T , LRG_524t1:c.4286G>T NP_000544.2:p.Gly1429Val
XM_011544639.1:c.4205G>T XP_011542941.1:p.Gly1402Val
XM_011544640.1:c.2687G>T XP_011542942.1:p.Gly896Val
XR_949643.1:n.88-1771C>A
XR_949644.1:n.88-1771C>A
XR_949645.1:n.88-1771C>A
XR_949646.1:n.88-1771C>A
XR_949647.1:n.701-1771C>A
XR_949648.1:n.603-1771C>A
NM_000553.5:c.4286G>T NP_000544.2:p.Gly1429Val
XM_011544639.3:c.4205G>T XP_011542941.1:p.Gly1402Val
XM_024447265.1:c.4076G>T XP_024303033.1:p.Gly1359Val
NM_000553.6:c.4286G>T MANE Select NP_000544.2:p.Gly1429Val