Canonical Allele Identifier: CA2667772060

Gene: TF

Linked Data

• gnomAD v4: 3-133775337-GCCCAGGTTCTCTA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133775339_133775351del , CM000665.2:g.133775339_133775351del	GRCh38
NC_000003.11:g.133494183_133494195del , CM000665.1:g.133494183_133494195del	GRCh37
NC_000003.10:g.134976873_134976885del	NCBI36
NG_013080.1:g.34207_34219del
NG_013080.2:g.118342_118354del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.1688-94_1688-82del MANE Select	ENSP00000385834.3:n.1688-94_1688-82del
ENST00000402696.7:c.1688-94_1688-82del	ENSP00000385834.3:n.1688-94_1688-82del
ENST00000461695.1:c.419-94_419-82del
ENST00000467842.1:n.2588_2600del
NM_001063.3:c.1688-94_1688-82del	NP_001054.1:n.1688-94_1688-82del
XM_011513100.1:c.1688-94_1688-82del	XP_011511402.1:n.1688-94_1688-82del
NM_001354703.1:c.1556-94_1556-82del	NP_001341632.1:n.1556-94_1556-82del
NM_001354704.1:c.1307-94_1307-82del	NP_001341633.1:n.1307-94_1307-82del
NM_001063.4:c.1688-94_1688-82del MANE Select	NP_001054.2:n.1688-94_1688-82del
NM_001354703.2:c.1556-94_1556-82del	NP_001341632.2:n.1556-94_1556-82del
NM_001354704.2:c.1307-94_1307-82del	NP_001341633.2:n.1307-94_1307-82del