Canonical Allele Identifier: CA2385822858
Gene: TIAM1 HGNC NCBI

Linked Data

dbSNP Id: rs2048471872

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.31545959G>A , CM000683.2:g.31545959G>A GRCh38
NC_000021.8:g.32918272G>A , CM000683.1:g.32918272G>A GRCh37
NC_000021.7:g.31840143G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000286827.7:c.-422+12968C>T ENSP00000286827.3:n.-422+12968C>T
ENST00000469412.5:n.59+13960C>T
ENST00000541036.5:c.-422+12968C>T ENSP00000441570.1:n.-422+12968C>T
NM_003253.2:c.-422+12968C>T NP_003244.2:n.-422+12968C>T
XM_011529711.1:c.-422+12629C>T XP_011528013.1:n.-422+12629C>T
XM_011529712.1:c.-422+13960C>T XP_011528014.1:n.-422+13960C>T
NM_001353688.1:c.-707+12968C>T NP_001340617.1:n.-707+12968C>T
NM_001353689.1:c.-489+12968C>T NP_001340618.1:n.-489+12968C>T
NM_001353690.1:c.-369+12968C>T NP_001340619.1:n.-369+12968C>T
NM_001353691.1:c.-518+12968C>T NP_001340620.1:n.-518+12968C>T
NM_001353692.1:c.-312+12968C>T NP_001340621.1:n.-312+12968C>T
NM_001353693.1:c.-422+12629C>T NP_001340622.1:n.-422+12629C>T
NM_003253.3:c.-422+12968C>T NP_003244.2:n.-422+12968C>T
XM_017028448.1:c.-489+12629C>T XP_016883937.1:n.-489+12629C>T
XM_024452127.1:c.-707+12629C>T XP_024307895.1:n.-707+12629C>T