Canonical Allele Identifier: CA899193491

Gene: TF

Linked Data

• dbSNP Id: rs1326038033
• gnomAD v3: 3-133757203-C-CT
• gnomAD v4: 3-133757203-C-CT
• MyVariant Identifiers: chr3:g.133476047_133476048insT (hg19) ; chr3:g.133757203_133757204insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133757204dup , CM000665.2:g.133757204dup	GRCh38
NC_000003.11:g.133476048dup , CM000665.1:g.133476048dup	GRCh37
NC_000003.10:g.134958738dup	NCBI36
NG_013080.1:g.16072dup
NG_013080.2:g.100207dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.870+195dup MANE Select	ENSP00000385834.3:n.870+195dup
ENST00000402696.7:c.870+195dup	ENSP00000385834.3:n.870+195dup
ENST00000485977.1:c.235+195dup	ENSP00000418716.1:n.235+195dup
NM_001063.3:c.870+195dup	NP_001054.1:n.870+195dup
XM_011513100.1:c.870+195dup	XP_011511402.1:n.870+195dup
NM_001354703.1:c.738+195dup	NP_001341632.1:n.738+195dup
NM_001354704.1:c.489+195dup	NP_001341633.1:n.489+195dup
NM_001063.4:c.870+195dup MANE Select	NP_001054.2:n.870+195dup
NM_001354703.2:c.738+195dup	NP_001341632.2:n.738+195dup
NM_001354704.2:c.489+195dup	NP_001341633.2:n.489+195dup