Canonical Allele Identifier: CA2667772097

Gene: TF

Linked Data

• gnomAD v4: 3-133775433-GA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133775439del , CM000665.2:g.133775439del	GRCh38
NC_000003.11:g.133494283del , CM000665.1:g.133494283del	GRCh37
NC_000003.10:g.134976973del	NCBI36
NG_013080.1:g.34307del
NG_013080.2:g.118442del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.1694del MANE Select	ENSP00000385834.3:p.Asn565ThrfsTer9
ENST00000402696.7:c.1694del	ENSP00000385834.3:p.Asn565ThrfsTer9
ENST00000461695.1:c.425del
ENST00000467842.1:n.2688del
NM_001063.3:c.1694del	NP_001054.1:p.Asn565ThrfsTer9
XM_011513100.1:c.1694del	XP_011511402.1:p.Asn565ThrfsTer9
NM_001354703.1:c.1562del	NP_001341632.1:p.Asn521ThrfsTer9
NM_001354704.1:c.1313del	NP_001341633.1:p.Asn438ThrfsTer9
NM_001063.4:c.1694del MANE Select	NP_001054.2:p.Asn565ThrfsTer9
NM_001354703.2:c.1562del	NP_001341632.2:p.Asn521ThrfsTer9
NM_001354704.2:c.1313del	NP_001341633.2:p.Asn438ThrfsTer9