Canonical Allele Identifier: CA2549199079

Gene: TIAM1

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.31545657_31545658insTCA , CM000683.2:g.31545657_31545658insTCA	GRCh38
NC_000021.8:g.32917970_32917971insTCA , CM000683.1:g.32917970_32917971insTCA	GRCh37
NC_000021.7:g.31839841_31839842insTCA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000286827.7:c.-422+13269_-422+13270insTGA	ENSP00000286827.3:n.-422+13269_-422+13270insTGA
ENST00000469412.5:n.59+14261_59+14262insTGA
ENST00000541036.5:c.-422+13269_-422+13270insTGA	ENSP00000441570.1:n.-422+13269_-422+13270insTGA
NM_003253.2:c.-422+13269_-422+13270insTGA	NP_003244.2:n.-422+13269_-422+13270insTGA
XM_011529711.1:c.-422+12930_-422+12931insTGA	XP_011528013.1:n.-422+12930_-422+12931insTGA
XM_011529712.1:c.-422+14261_-422+14262insTGA	XP_011528014.1:n.-422+14261_-422+14262insTGA
NM_001353688.1:c.-707+13269_-707+13270insTGA	NP_001340617.1:n.-707+13269_-707+13270insTGA
NM_001353689.1:c.-489+13269_-489+13270insTGA	NP_001340618.1:n.-489+13269_-489+13270insTGA
NM_001353690.1:c.-369+13269_-369+13270insTGA	NP_001340619.1:n.-369+13269_-369+13270insTGA
NM_001353691.1:c.-518+13269_-518+13270insTGA	NP_001340620.1:n.-518+13269_-518+13270insTGA
NM_001353692.1:c.-312+13269_-312+13270insTGA	NP_001340621.1:n.-312+13269_-312+13270insTGA
NM_001353693.1:c.-422+12930_-422+12931insTGA	NP_001340622.1:n.-422+12930_-422+12931insTGA
NM_003253.3:c.-422+13269_-422+13270insTGA	NP_003244.2:n.-422+13269_-422+13270insTGA
XM_017028448.1:c.-489+12930_-489+12931insTGA	XP_016883937.1:n.-489+12930_-489+12931insTGA
XM_024452127.1:c.-707+12930_-707+12931insTGA	XP_024307895.1:n.-707+12930_-707+12931insTGA