Canonical Allele Identifier: CA2667772159

Gene: TF

Linked Data

• gnomAD v4: 3-133775742-T-TGGCA

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133775742_133775743insGGCA , CM000665.2:g.133775742_133775743insGGCA	GRCh38
NC_000003.11:g.133494586_133494587insGGCA , CM000665.1:g.133494586_133494587insGGCA	GRCh37
NC_000003.10:g.134977276_134977277insGGCA	NCBI36
NG_013080.1:g.34610_34611insGGCA
NG_013080.2:g.118745_118746insGGCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.1872+125_1872+126insGGCA MANE Select	ENSP00000385834.3:n.1872+125_1872+126insGGCA
ENST00000402696.7:c.1872+125_1872+126insGGCA	ENSP00000385834.3:n.1872+125_1872+126insGGCA
ENST00000461695.1:c.603+125_603+126insGGCA
ENST00000467842.1:n.2866+125_2866+126insGGCA
NM_001063.3:c.1872+125_1872+126insGGCA	NP_001054.1:n.1872+125_1872+126insGGCA
XM_011513100.1:c.1872+125_1872+126insGGCA	XP_011511402.1:n.1872+125_1872+126insGGCA
NM_001354703.1:c.1740+125_1740+126insGGCA	NP_001341632.1:n.1740+125_1740+126insGGCA
NM_001354704.1:c.1491+125_1491+126insGGCA	NP_001341633.1:n.1491+125_1491+126insGGCA
NM_001063.4:c.1872+125_1872+126insGGCA MANE Select	NP_001054.2:n.1872+125_1872+126insGGCA
NM_001354703.2:c.1740+125_1740+126insGGCA	NP_001341632.2:n.1740+125_1740+126insGGCA
NM_001354704.2:c.1491+125_1491+126insGGCA	NP_001341633.2:n.1491+125_1491+126insGGCA