Canonical Allele Identifier: CA546420502

Gene: TF

Linked Data

• dbSNP Id: rs1386762652
• gnomAD v2: 3-133476042-A-ACCGTCTGCCGCCC
• gnomAD v3: 3-133757198-A-ACCGTCTGCCGCCC
• gnomAD v4: 3-133757198-A-ACCGTCTGCCGCCC
• MyVariant Identifiers: chr3:g.133476042_133476043insCCGTCTGCCGCCC (hg19) ; chr3:g.133757198_133757199insCCGTCTGCCGCCC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133757199_133757211dup , CM000665.2:g.133757199_133757211dup	GRCh38
NC_000003.11:g.133476043_133476055dup , CM000665.1:g.133476043_133476055dup	GRCh37
NC_000003.10:g.134958733_134958745dup	NCBI36
NG_013080.1:g.16067_16079dup
NG_013080.2:g.100202_100214dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.870+190_870+202dup MANE Select	ENSP00000385834.3:n.870+190_870+202dup
ENST00000402696.7:c.870+190_870+202dup	ENSP00000385834.3:n.870+190_870+202dup
ENST00000485977.1:c.235+190_235+202dup	ENSP00000418716.1:n.235+190_235+202dup
NM_001063.3:c.870+190_870+202dup	NP_001054.1:n.870+190_870+202dup
XM_011513100.1:c.870+190_870+202dup	XP_011511402.1:n.870+190_870+202dup
NM_001354703.1:c.738+190_738+202dup	NP_001341632.1:n.738+190_738+202dup
NM_001354704.1:c.489+190_489+202dup	NP_001341633.1:n.489+190_489+202dup
NM_001063.4:c.870+190_870+202dup MANE Select	NP_001054.2:n.870+190_870+202dup
NM_001354703.2:c.738+190_738+202dup	NP_001341632.2:n.738+190_738+202dup
NM_001354704.2:c.489+190_489+202dup	NP_001341633.2:n.489+190_489+202dup