Canonical Allele Identifier: CA2686840620
Gene: WRN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.31173173_31173174insTGAAGTCT , CM000670.2:g.31173173_31173174insTGAAGTCT GRCh38
NC_000008.10:g.31030689_31030690insTGAAGTCT , CM000670.1:g.31030689_31030690insTGAAGTCT GRCh37
NC_000008.9:g.31150231_31150232insTGAAGTCT NCBI36
NG_008870.1:g.144912_144913insTGAAGTCT , LRG_524:g.144912_144913insTGAAGTCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000298139.7:c.*71_*72insTGAAGTCT MANE Select ENSP00000298139.5:n.*71_*72insTGAAGTCT
ENST00000650667.1:c.*3984_*3985insTGAAGTCT ENSP00000498593.1:n.*3984_*3985insTGAAGTCT
ENST00000651946.1:n.594_595insTGAAGTCT
ENST00000298139.5:c.*71_*72insTGAAGTCT ENSP00000298139.5:n.*71_*72insTGAAGTCT
ENST00000521620.5:n.3003_3004insTGAAGTCT
NM_000553.4:c.*71_*72insTGAAGTCT , LRG_524t1:c.*71_*72insTGAAGTCT NP_000544.2:n.*71_*72insTGAAGTCT
XM_011544639.1:c.*71_*72insTGAAGTCT XP_011542941.1:n.*71_*72insTGAAGTCT
XM_011544640.1:c.*71_*72insTGAAGTCT XP_011542942.1:n.*71_*72insTGAAGTCT
XR_949643.1:n.88-1856_88-1855insAGACTTCA
XR_949644.1:n.88-1856_88-1855insAGACTTCA
XR_949645.1:n.88-1856_88-1855insAGACTTCA
XR_949646.1:n.88-1856_88-1855insAGACTTCA
XR_949647.1:n.701-1856_701-1855insAGACTTCA
XR_949648.1:n.603-1856_603-1855insAGACTTCA
NM_000553.5:c.*71_*72insTGAAGTCT NP_000544.2:n.*71_*72insTGAAGTCT
XM_011544639.3:c.*71_*72insTGAAGTCT XP_011542941.1:n.*71_*72insTGAAGTCT
XM_024447265.1:c.*71_*72insTGAAGTCT XP_024303033.1:n.*71_*72insTGAAGTCT
NM_000553.6:c.*71_*72insTGAAGTCT MANE Select NP_000544.2:n.*71_*72insTGAAGTCT