Canonical Allele Identifier: CA2667772052

Gene: TF

Linked Data

• gnomAD v4: 3-133775323-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133775324del , CM000665.2:g.133775324del	GRCh38
NC_000003.11:g.133494168del , CM000665.1:g.133494168del	GRCh37
NC_000003.10:g.134976858del	NCBI36
NG_013080.1:g.34192del
NG_013080.2:g.118327del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.1688-109del MANE Select	ENSP00000385834.3:n.1688-109del
ENST00000402696.7:c.1688-109del	ENSP00000385834.3:n.1688-109del
ENST00000461695.1:c.419-109del
ENST00000467842.1:n.2573del
NM_001063.3:c.1688-109del	NP_001054.1:n.1688-109del
XM_011513100.1:c.1688-109del	XP_011511402.1:n.1688-109del
NM_001354703.1:c.1556-109del	NP_001341632.1:n.1556-109del
NM_001354704.1:c.1307-109del	NP_001341633.1:n.1307-109del
NM_001063.4:c.1688-109del MANE Select	NP_001054.2:n.1688-109del
NM_001354703.2:c.1556-109del	NP_001341632.2:n.1556-109del
NM_001354704.2:c.1307-109del	NP_001341633.2:n.1307-109del