Canonical Allele Identifier: CA2385822934
Gene: TIAM1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.31546099_31546102delinsTAAC , CM000683.2:g.31546099_31546102delinsTAAC GRCh38
NC_000021.8:g.32918412_32918415delinsTAAC , CM000683.1:g.32918412_32918415delinsTAAC GRCh37
NC_000021.7:g.31840283_31840286delinsTAAC NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000286827.7:c.-422+12825_-422+12828delinsGTTA ENSP00000286827.3:n.-422+12825_-422+12828delinsGTTA
ENST00000469412.5:n.59+13817_59+13820delinsGTTA
ENST00000541036.5:c.-422+12825_-422+12828delinsGTTA ENSP00000441570.1:n.-422+12825_-422+12828delinsGTTA
NM_003253.2:c.-422+12825_-422+12828delinsGTTA NP_003244.2:n.-422+12825_-422+12828delinsGTTA
XM_011529711.1:c.-422+12486_-422+12489delinsGTTA XP_011528013.1:n.-422+12486_-422+12489delinsGTTA
XM_011529712.1:c.-422+13817_-422+13820delinsGTTA XP_011528014.1:n.-422+13817_-422+13820delinsGTTA
NM_001353688.1:c.-707+12825_-707+12828delinsGTTA NP_001340617.1:n.-707+12825_-707+12828delinsGTTA
NM_001353689.1:c.-489+12825_-489+12828delinsGTTA NP_001340618.1:n.-489+12825_-489+12828delinsGTTA
NM_001353690.1:c.-369+12825_-369+12828delinsGTTA NP_001340619.1:n.-369+12825_-369+12828delinsGTTA
NM_001353691.1:c.-518+12825_-518+12828delinsGTTA NP_001340620.1:n.-518+12825_-518+12828delinsGTTA
NM_001353692.1:c.-312+12825_-312+12828delinsGTTA NP_001340621.1:n.-312+12825_-312+12828delinsGTTA
NM_001353693.1:c.-422+12486_-422+12489delinsGTTA NP_001340622.1:n.-422+12486_-422+12489delinsGTTA
NM_003253.3:c.-422+12825_-422+12828delinsGTTA NP_003244.2:n.-422+12825_-422+12828delinsGTTA
XM_017028448.1:c.-489+12486_-489+12489delinsGTTA XP_016883937.1:n.-489+12486_-489+12489delinsGTTA
XM_024452127.1:c.-707+12486_-707+12489delinsGTTA XP_024307895.1:n.-707+12486_-707+12489delinsGTTA