Canonical Allele Identifier: CA1403130629

Gene: TF

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133775327_133775335delinsTGGCGAGAA , CM000665.2:g.133775327_133775335delinsTGGCGAGAA	GRCh38
NC_000003.11:g.133494171_133494179delinsTGGCGAGAA , CM000665.1:g.133494171_133494179delinsTGGCGAGAA	GRCh37
NC_000003.10:g.134976861_134976869delinsTGGCGAGAA	NCBI36
NG_013080.1:g.34195_34203delinsTGGCGAGAA
NG_013080.2:g.118330_118338delinsTGGCGAGAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.1688-106_1688-98delinsTGGCGAGAA MANE Select	ENSP00000385834.3:n.1688-106_1688-98delinsTGGCGAGAA
ENST00000402696.7:c.1688-106_1688-98delinsTGGCGAGAA	ENSP00000385834.3:n.1688-106_1688-98delinsTGGCGAGAA
ENST00000461695.1:c.419-106_419-98delinsTGGCGAGAA
ENST00000467842.1:n.2576_2584delinsTGGCGAGAA
NM_001063.3:c.1688-106_1688-98delinsTGGCGAGAA	NP_001054.1:n.1688-106_1688-98delinsTGGCGAGAA
XM_011513100.1:c.1688-106_1688-98delinsTGGCGAGAA	XP_011511402.1:n.1688-106_1688-98delinsTGGCGAGAA
NM_001354703.1:c.1556-106_1556-98delinsTGGCGAGAA	NP_001341632.1:n.1556-106_1556-98delinsTGGCGAGAA
NM_001354704.1:c.1307-106_1307-98delinsTGGCGAGAA	NP_001341633.1:n.1307-106_1307-98delinsTGGCGAGAA
NM_001063.4:c.1688-106_1688-98delinsTGGCGAGAA MANE Select	NP_001054.2:n.1688-106_1688-98delinsTGGCGAGAA
NM_001354703.2:c.1556-106_1556-98delinsTGGCGAGAA	NP_001341632.2:n.1556-106_1556-98delinsTGGCGAGAA
NM_001354704.2:c.1307-106_1307-98delinsTGGCGAGAA	NP_001341633.2:n.1307-106_1307-98delinsTGGCGAGAA