Canonical Allele Identifier: CA2385822842

Gene: TIAM1

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.31545931G= , CM000683.2:g.31545931G=	GRCh38
NC_000021.8:g.32918244G= , CM000683.1:g.32918244G=	GRCh37
NC_000021.7:g.31840115G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000286827.7:c.-422+12996C=	ENSP00000286827.3:n.-422+12996C=
ENST00000469412.5:n.59+13988C=
ENST00000541036.5:c.-422+12996C=	ENSP00000441570.1:n.-422+12996C=
NM_003253.2:c.-422+12996C=	NP_003244.2:n.-422+12996C=
XM_011529711.1:c.-422+12657C=	XP_011528013.1:n.-422+12657C=
XM_011529712.1:c.-422+13988C=	XP_011528014.1:n.-422+13988C=
NM_001353688.1:c.-707+12996C=	NP_001340617.1:n.-707+12996C=
NM_001353689.1:c.-489+12996C=	NP_001340618.1:n.-489+12996C=
NM_001353690.1:c.-369+12996C=	NP_001340619.1:n.-369+12996C=
NM_001353691.1:c.-518+12996C=	NP_001340620.1:n.-518+12996C=
NM_001353692.1:c.-312+12996C=	NP_001340621.1:n.-312+12996C=
NM_001353693.1:c.-422+12657C=	NP_001340622.1:n.-422+12657C=
NM_003253.3:c.-422+12996C=	NP_003244.2:n.-422+12996C=
XM_017028448.1:c.-489+12657C=	XP_016883937.1:n.-489+12657C=
XM_024452127.1:c.-707+12657C=	XP_024307895.1:n.-707+12657C=