Canonical Allele Identifier: CA320027715

Gene: TIAM1

Linked Data

• dbSNP Id: rs779458931
• gnomAD v2: 21-32918138-A-T
• gnomAD v3: 21-31545825-A-T
• gnomAD v4: 21-31545825-A-T
• MyVariant Identifiers: chr21:g.32918138A>T (hg19) ; chr21:g.31545825A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.31545825A>T , CM000683.2:g.31545825A>T	GRCh38
NC_000021.8:g.32918138A>T , CM000683.1:g.32918138A>T	GRCh37
NC_000021.7:g.31840009A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000286827.7:c.-422+13102T>A	ENSP00000286827.3:n.-422+13102T>A
ENST00000469412.5:n.59+14094T>A
ENST00000541036.5:c.-422+13102T>A	ENSP00000441570.1:n.-422+13102T>A
NM_003253.2:c.-422+13102T>A	NP_003244.2:n.-422+13102T>A
XM_011529711.1:c.-422+12763T>A	XP_011528013.1:n.-422+12763T>A
XM_011529712.1:c.-422+14094T>A	XP_011528014.1:n.-422+14094T>A
NM_001353688.1:c.-707+13102T>A	NP_001340617.1:n.-707+13102T>A
NM_001353689.1:c.-489+13102T>A	NP_001340618.1:n.-489+13102T>A
NM_001353690.1:c.-369+13102T>A	NP_001340619.1:n.-369+13102T>A
NM_001353691.1:c.-518+13102T>A	NP_001340620.1:n.-518+13102T>A
NM_001353692.1:c.-312+13102T>A	NP_001340621.1:n.-312+13102T>A
NM_001353693.1:c.-422+12763T>A	NP_001340622.1:n.-422+12763T>A
NM_003253.3:c.-422+13102T>A	NP_003244.2:n.-422+13102T>A
XM_017028448.1:c.-489+12763T>A	XP_016883937.1:n.-489+12763T>A
XM_024452127.1:c.-707+12763T>A	XP_024307895.1:n.-707+12763T>A