Canonical Allele Identifier: CA748674850

Gene: TIAM1

Linked Data

• dbSNP Id: rs1422945228
• gnomAD v3: 21-31545725-A-ATCAC
• gnomAD v4: 21-31545725-A-ATCAC
• MyVariant Identifiers: chr21:g.32918038_32918039insTCAC (hg19) ; chr21:g.31545725_31545726insTCAC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.31545727_31545730dup , CM000683.2:g.31545727_31545730dup	GRCh38
NC_000021.8:g.32918040_32918043dup , CM000683.1:g.32918040_32918043dup	GRCh37
NC_000021.7:g.31839911_31839914dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000286827.7:c.-422+13198_-422+13201dup	ENSP00000286827.3:n.-422+13198_-422+13201dup
ENST00000469412.5:n.59+14190_59+14193dup
ENST00000541036.5:c.-422+13198_-422+13201dup	ENSP00000441570.1:n.-422+13198_-422+13201dup
NM_003253.2:c.-422+13198_-422+13201dup	NP_003244.2:n.-422+13198_-422+13201dup
XM_011529711.1:c.-422+12859_-422+12862dup	XP_011528013.1:n.-422+12859_-422+12862dup
XM_011529712.1:c.-422+14190_-422+14193dup	XP_011528014.1:n.-422+14190_-422+14193dup
NM_001353688.1:c.-707+13198_-707+13201dup	NP_001340617.1:n.-707+13198_-707+13201dup
NM_001353689.1:c.-489+13198_-489+13201dup	NP_001340618.1:n.-489+13198_-489+13201dup
NM_001353690.1:c.-369+13198_-369+13201dup	NP_001340619.1:n.-369+13198_-369+13201dup
NM_001353691.1:c.-518+13198_-518+13201dup	NP_001340620.1:n.-518+13198_-518+13201dup
NM_001353692.1:c.-312+13198_-312+13201dup	NP_001340621.1:n.-312+13198_-312+13201dup
NM_001353693.1:c.-422+12859_-422+12862dup	NP_001340622.1:n.-422+12859_-422+12862dup
NM_003253.3:c.-422+13198_-422+13201dup	NP_003244.2:n.-422+13198_-422+13201dup
XM_017028448.1:c.-489+12859_-489+12862dup	XP_016883937.1:n.-489+12859_-489+12862dup
XM_024452127.1:c.-707+12859_-707+12862dup	XP_024307895.1:n.-707+12859_-707+12862dup