Canonical Allele Identifier: CA2385822772
Gene: TIAM1 HGNC NCBI

Linked Data

dbSNP Id: rs2048465690

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.31545749_31545752dup , CM000683.2:g.31545749_31545752dup GRCh38
NC_000021.8:g.32918062_32918065dup , CM000683.1:g.32918062_32918065dup GRCh37
NC_000021.7:g.31839933_31839936dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000286827.7:c.-422+13175_-422+13178dup ENSP00000286827.3:n.-422+13175_-422+13178dup
ENST00000469412.5:n.59+14167_59+14170dup
ENST00000541036.5:c.-422+13175_-422+13178dup ENSP00000441570.1:n.-422+13175_-422+13178dup
NM_003253.2:c.-422+13175_-422+13178dup NP_003244.2:n.-422+13175_-422+13178dup
XM_011529711.1:c.-422+12836_-422+12839dup XP_011528013.1:n.-422+12836_-422+12839dup
XM_011529712.1:c.-422+14167_-422+14170dup XP_011528014.1:n.-422+14167_-422+14170dup
NM_001353688.1:c.-707+13175_-707+13178dup NP_001340617.1:n.-707+13175_-707+13178dup
NM_001353689.1:c.-489+13175_-489+13178dup NP_001340618.1:n.-489+13175_-489+13178dup
NM_001353690.1:c.-369+13175_-369+13178dup NP_001340619.1:n.-369+13175_-369+13178dup
NM_001353691.1:c.-518+13175_-518+13178dup NP_001340620.1:n.-518+13175_-518+13178dup
NM_001353692.1:c.-312+13175_-312+13178dup NP_001340621.1:n.-312+13175_-312+13178dup
NM_001353693.1:c.-422+12836_-422+12839dup NP_001340622.1:n.-422+12836_-422+12839dup
NM_003253.3:c.-422+13175_-422+13178dup NP_003244.2:n.-422+13175_-422+13178dup
XM_017028448.1:c.-489+12836_-489+12839dup XP_016883937.1:n.-489+12836_-489+12839dup
XM_024452127.1:c.-707+12836_-707+12839dup XP_024307895.1:n.-707+12836_-707+12839dup