Canonical Allele Identifier: CA2385822789
Gene: TIAM1 HGNC NCBI

Linked Data

dbSNP Id: rs2048466889

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.31545794C>A , CM000683.2:g.31545794C>A GRCh38
NC_000021.8:g.32918107C>A , CM000683.1:g.32918107C>A GRCh37
NC_000021.7:g.31839978C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000286827.7:c.-422+13133G>T ENSP00000286827.3:n.-422+13133G>T
ENST00000469412.5:n.59+14125G>T
ENST00000541036.5:c.-422+13133G>T ENSP00000441570.1:n.-422+13133G>T
NM_003253.2:c.-422+13133G>T NP_003244.2:n.-422+13133G>T
XM_011529711.1:c.-422+12794G>T XP_011528013.1:n.-422+12794G>T
XM_011529712.1:c.-422+14125G>T XP_011528014.1:n.-422+14125G>T
NM_001353688.1:c.-707+13133G>T NP_001340617.1:n.-707+13133G>T
NM_001353689.1:c.-489+13133G>T NP_001340618.1:n.-489+13133G>T
NM_001353690.1:c.-369+13133G>T NP_001340619.1:n.-369+13133G>T
NM_001353691.1:c.-518+13133G>T NP_001340620.1:n.-518+13133G>T
NM_001353692.1:c.-312+13133G>T NP_001340621.1:n.-312+13133G>T
NM_001353693.1:c.-422+12794G>T NP_001340622.1:n.-422+12794G>T
NM_003253.3:c.-422+13133G>T NP_003244.2:n.-422+13133G>T
XM_017028448.1:c.-489+12794G>T XP_016883937.1:n.-489+12794G>T
XM_024452127.1:c.-707+12794G>T XP_024307895.1:n.-707+12794G>T