Canonical Allele Identifier: CA748674948
Gene: TIAM1 HGNC NCBI

Linked Data

dbSNP Id: rs1255553719

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.31546101_31546104del , CM000683.2:g.31546101_31546104del GRCh38
NC_000021.8:g.32918414_32918417del , CM000683.1:g.32918414_32918417del GRCh37
NC_000021.7:g.31840285_31840288del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000286827.7:c.-422+12824_-422+12827del ENSP00000286827.3:n.-422+12824_-422+12827del
ENST00000469412.5:n.59+13816_59+13819del
ENST00000541036.5:c.-422+12824_-422+12827del ENSP00000441570.1:n.-422+12824_-422+12827del
NM_003253.2:c.-422+12824_-422+12827del NP_003244.2:n.-422+12824_-422+12827del
XM_011529711.1:c.-422+12485_-422+12488del XP_011528013.1:n.-422+12485_-422+12488del
XM_011529712.1:c.-422+13816_-422+13819del XP_011528014.1:n.-422+13816_-422+13819del
NM_001353688.1:c.-707+12824_-707+12827del NP_001340617.1:n.-707+12824_-707+12827del
NM_001353689.1:c.-489+12824_-489+12827del NP_001340618.1:n.-489+12824_-489+12827del
NM_001353690.1:c.-369+12824_-369+12827del NP_001340619.1:n.-369+12824_-369+12827del
NM_001353691.1:c.-518+12824_-518+12827del NP_001340620.1:n.-518+12824_-518+12827del
NM_001353692.1:c.-312+12824_-312+12827del NP_001340621.1:n.-312+12824_-312+12827del
NM_001353693.1:c.-422+12485_-422+12488del NP_001340622.1:n.-422+12485_-422+12488del
NM_003253.3:c.-422+12824_-422+12827del NP_003244.2:n.-422+12824_-422+12827del
XM_017028448.1:c.-489+12485_-489+12488del XP_016883937.1:n.-489+12485_-489+12488del
XM_024452127.1:c.-707+12485_-707+12488del XP_024307895.1:n.-707+12485_-707+12488del