Canonical Allele Identifier: CA2817699200
Gene: TIAM1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.31545866_31545873del , CM000683.2:g.31545866_31545873del GRCh38
NC_000021.8:g.32918179_32918186del , CM000683.1:g.32918179_32918186del GRCh37
NC_000021.7:g.31840050_31840057del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000286827.7:c.-422+13055_-422+13062del ENSP00000286827.3:n.-422+13055_-422+13062del
ENST00000469412.5:n.59+14047_59+14054del
ENST00000541036.5:c.-422+13055_-422+13062del ENSP00000441570.1:n.-422+13055_-422+13062del
NM_003253.2:c.-422+13055_-422+13062del NP_003244.2:n.-422+13055_-422+13062del
XM_011529711.1:c.-422+12716_-422+12723del XP_011528013.1:n.-422+12716_-422+12723del
XM_011529712.1:c.-422+14047_-422+14054del XP_011528014.1:n.-422+14047_-422+14054del
NM_001353688.1:c.-707+13055_-707+13062del NP_001340617.1:n.-707+13055_-707+13062del
NM_001353689.1:c.-489+13055_-489+13062del NP_001340618.1:n.-489+13055_-489+13062del
NM_001353690.1:c.-369+13055_-369+13062del NP_001340619.1:n.-369+13055_-369+13062del
NM_001353691.1:c.-518+13055_-518+13062del NP_001340620.1:n.-518+13055_-518+13062del
NM_001353692.1:c.-312+13055_-312+13062del NP_001340621.1:n.-312+13055_-312+13062del
NM_001353693.1:c.-422+12716_-422+12723del NP_001340622.1:n.-422+12716_-422+12723del
NM_003253.3:c.-422+13055_-422+13062del NP_003244.2:n.-422+13055_-422+13062del
XM_017028448.1:c.-489+12716_-489+12723del XP_016883937.1:n.-489+12716_-489+12723del
XM_024452127.1:c.-707+12716_-707+12723del XP_024307895.1:n.-707+12716_-707+12723del