Canonical Allele Identifier: CA2385822883

Gene: TIAM1

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.31546004_31546005delinsGA , CM000683.2:g.31546004_31546005delinsGA	GRCh38
NC_000021.8:g.32918317_32918318delinsGA , CM000683.1:g.32918317_32918318delinsGA	GRCh37
NC_000021.7:g.31840188_31840189delinsGA	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000286827.7:c.-422+12922_-422+12923delinsTC	ENSP00000286827.3:n.-422+12922_-422+12923delinsTC
ENST00000469412.5:n.59+13914_59+13915delinsTC
ENST00000541036.5:c.-422+12922_-422+12923delinsTC	ENSP00000441570.1:n.-422+12922_-422+12923delinsTC
NM_003253.2:c.-422+12922_-422+12923delinsTC	NP_003244.2:n.-422+12922_-422+12923delinsTC
XM_011529711.1:c.-422+12583_-422+12584delinsTC	XP_011528013.1:n.-422+12583_-422+12584delinsTC
XM_011529712.1:c.-422+13914_-422+13915delinsTC	XP_011528014.1:n.-422+13914_-422+13915delinsTC
NM_001353688.1:c.-707+12922_-707+12923delinsTC	NP_001340617.1:n.-707+12922_-707+12923delinsTC
NM_001353689.1:c.-489+12922_-489+12923delinsTC	NP_001340618.1:n.-489+12922_-489+12923delinsTC
NM_001353690.1:c.-369+12922_-369+12923delinsTC	NP_001340619.1:n.-369+12922_-369+12923delinsTC
NM_001353691.1:c.-518+12922_-518+12923delinsTC	NP_001340620.1:n.-518+12922_-518+12923delinsTC
NM_001353692.1:c.-312+12922_-312+12923delinsTC	NP_001340621.1:n.-312+12922_-312+12923delinsTC
NM_001353693.1:c.-422+12583_-422+12584delinsTC	NP_001340622.1:n.-422+12583_-422+12584delinsTC
NM_003253.3:c.-422+12922_-422+12923delinsTC	NP_003244.2:n.-422+12922_-422+12923delinsTC
XM_017028448.1:c.-489+12583_-489+12584delinsTC	XP_016883937.1:n.-489+12583_-489+12584delinsTC
XM_024452127.1:c.-707+12583_-707+12584delinsTC	XP_024307895.1:n.-707+12583_-707+12584delinsTC