Canonical Allele Identifier: CA2667771998

Gene: TF

Linked Data

• gnomAD v4: 3-133775253-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133775255del , CM000665.2:g.133775255del	GRCh38
NC_000003.11:g.133494099del , CM000665.1:g.133494099del	GRCh37
NC_000003.10:g.134976789del	NCBI36
NG_013080.1:g.34123del
NG_013080.2:g.118258del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.1688-178del MANE Select	ENSP00000385834.3:n.1688-178del
ENST00000402696.7:c.1688-178del	ENSP00000385834.3:n.1688-178del
ENST00000461695.1:c.419-178del
ENST00000467842.1:n.2504del
NM_001063.3:c.1688-178del	NP_001054.1:n.1688-178del
XM_011513100.1:c.1688-178del	XP_011511402.1:n.1688-178del
NM_001354703.1:c.1556-178del	NP_001341632.1:n.1556-178del
NM_001354704.1:c.1307-178del	NP_001341633.1:n.1307-178del
NM_001063.4:c.1688-178del MANE Select	NP_001054.2:n.1688-178del
NM_001354703.2:c.1556-178del	NP_001341632.2:n.1556-178del
NM_001354704.2:c.1307-178del	NP_001341633.2:n.1307-178del