Canonical Allele Identifier: CA1403130642

Gene: TF

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133775343_133775344delinsGT , CM000665.2:g.133775343_133775344delinsGT	GRCh38
NC_000003.11:g.133494187_133494188delinsGT , CM000665.1:g.133494187_133494188delinsGT	GRCh37
NC_000003.10:g.134976877_134976878delinsGT	NCBI36
NG_013080.1:g.34211_34212delinsGT
NG_013080.2:g.118346_118347delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.1688-90_1688-89delinsGT MANE Select	ENSP00000385834.3:n.1688-90_1688-89delinsGT
ENST00000402696.7:c.1688-90_1688-89delinsGT	ENSP00000385834.3:n.1688-90_1688-89delinsGT
ENST00000461695.1:c.419-90_419-89delinsGT
ENST00000467842.1:n.2592_2593delinsGT
NM_001063.3:c.1688-90_1688-89delinsGT	NP_001054.1:n.1688-90_1688-89delinsGT
XM_011513100.1:c.1688-90_1688-89delinsGT	XP_011511402.1:n.1688-90_1688-89delinsGT
NM_001354703.1:c.1556-90_1556-89delinsGT	NP_001341632.1:n.1556-90_1556-89delinsGT
NM_001354704.1:c.1307-90_1307-89delinsGT	NP_001341633.1:n.1307-90_1307-89delinsGT
NM_001063.4:c.1688-90_1688-89delinsGT MANE Select	NP_001054.2:n.1688-90_1688-89delinsGT
NM_001354703.2:c.1556-90_1556-89delinsGT	NP_001341632.2:n.1556-90_1556-89delinsGT
NM_001354704.2:c.1307-90_1307-89delinsGT	NP_001341633.2:n.1307-90_1307-89delinsGT