Canonical Allele Identifier: CA2667772044

Gene: TF

Linked Data

• gnomAD v4: 3-133775310-AG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133775311del , CM000665.2:g.133775311del	GRCh38
NC_000003.11:g.133494155del , CM000665.1:g.133494155del	GRCh37
NC_000003.10:g.134976845del	NCBI36
NG_013080.1:g.34179del
NG_013080.2:g.118314del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.1688-122del MANE Select	ENSP00000385834.3:n.1688-122del
ENST00000402696.7:c.1688-122del	ENSP00000385834.3:n.1688-122del
ENST00000461695.1:c.419-122del
ENST00000467842.1:n.2560del
NM_001063.3:c.1688-122del	NP_001054.1:n.1688-122del
XM_011513100.1:c.1688-122del	XP_011511402.1:n.1688-122del
NM_001354703.1:c.1556-122del	NP_001341632.1:n.1556-122del
NM_001354704.1:c.1307-122del	NP_001341633.1:n.1307-122del
NM_001063.4:c.1688-122del MANE Select	NP_001054.2:n.1688-122del
NM_001354703.2:c.1556-122del	NP_001341632.2:n.1556-122del
NM_001354704.2:c.1307-122del	NP_001341633.2:n.1307-122del