Canonical Allele Identifier: CA2817699202
Gene: TIAM1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.31545897_31545898dup , CM000683.2:g.31545897_31545898dup GRCh38
NC_000021.8:g.32918210_32918211dup , CM000683.1:g.32918210_32918211dup GRCh37
NC_000021.7:g.31840081_31840082dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000286827.7:c.-422+13029_-422+13030dup ENSP00000286827.3:n.-422+13029_-422+13030dup
ENST00000469412.5:n.59+14021_59+14022dup
ENST00000541036.5:c.-422+13029_-422+13030dup ENSP00000441570.1:n.-422+13029_-422+13030dup
NM_003253.2:c.-422+13029_-422+13030dup NP_003244.2:n.-422+13029_-422+13030dup
XM_011529711.1:c.-422+12690_-422+12691dup XP_011528013.1:n.-422+12690_-422+12691dup
XM_011529712.1:c.-422+14021_-422+14022dup XP_011528014.1:n.-422+14021_-422+14022dup
NM_001353688.1:c.-707+13029_-707+13030dup NP_001340617.1:n.-707+13029_-707+13030dup
NM_001353689.1:c.-489+13029_-489+13030dup NP_001340618.1:n.-489+13029_-489+13030dup
NM_001353690.1:c.-369+13029_-369+13030dup NP_001340619.1:n.-369+13029_-369+13030dup
NM_001353691.1:c.-518+13029_-518+13030dup NP_001340620.1:n.-518+13029_-518+13030dup
NM_001353692.1:c.-312+13029_-312+13030dup NP_001340621.1:n.-312+13029_-312+13030dup
NM_001353693.1:c.-422+12690_-422+12691dup NP_001340622.1:n.-422+12690_-422+12691dup
NM_003253.3:c.-422+13029_-422+13030dup NP_003244.2:n.-422+13029_-422+13030dup
XM_017028448.1:c.-489+12690_-489+12691dup XP_016883937.1:n.-489+12690_-489+12691dup
XM_024452127.1:c.-707+12690_-707+12691dup XP_024307895.1:n.-707+12690_-707+12691dup