Canonical Allele Identifier: CA4704754
Gene: WRN HGNC NCBI

Linked Data

dbSNP Id: rs747315984
gnomAD v2: 8-30977713-A-T
gnomAD v3: 8-31120197-A-T
gnomAD v4: 8-31120197-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.31120197A>T , CM000670.2:g.31120197A>T GRCh38
NC_000008.10:g.30977713A>T , CM000670.1:g.30977713A>T GRCh37
NC_000008.9:g.31097255A>T NCBI36
NG_008870.1:g.91936A>T , LRG_524:g.91936A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000298139.7:c.2449-46A>T MANE Select ENSP00000298139.5:n.2449-46A>T
ENST00000650667.1:c.*2063-46A>T ENSP00000498593.1:n.*2063-46A>T
ENST00000298139.5:c.2449-46A>T ENSP00000298139.5:n.2449-46A>T
ENST00000520169.1:n.242A>T
ENST00000521620.5:n.1082-46A>T
NM_000553.4:c.2449-46A>T , LRG_524t1:c.2449-46A>T NP_000544.2:n.2449-46A>T
XM_011544639.1:c.2368-46A>T XP_011542941.1:n.2368-46A>T
XM_011544640.1:c.850-46A>T XP_011542942.1:n.850-46A>T
XR_949470.1:n.2722-46A>T
XR_949471.1:n.2722-46A>T
XR_949472.1:n.2722-46A>T
NM_000553.5:c.2449-46A>T NP_000544.2:n.2449-46A>T
XM_011544639.3:c.2368-46A>T XP_011542941.1:n.2368-46A>T
XM_024447265.1:c.2239-46A>T XP_024303033.1:n.2239-46A>T
XR_949470.3:n.2750-46A>T
XR_949471.3:n.2750-46A>T
XR_949472.3:n.2750-46A>T
NM_000553.6:c.2449-46A>T MANE Select NP_000544.2:n.2449-46A>T