Canonical Allele Identifier: CA2667772086

Gene: TF

Linked Data

• gnomAD v4: 3-133775389-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133775391del , CM000665.2:g.133775391del	GRCh38
NC_000003.11:g.133494235del , CM000665.1:g.133494235del	GRCh37
NC_000003.10:g.134976925del	NCBI36
NG_013080.1:g.34259del
NG_013080.2:g.118394del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.1688-42del MANE Select	ENSP00000385834.3:n.1688-42del
ENST00000402696.7:c.1688-42del	ENSP00000385834.3:n.1688-42del
ENST00000461695.1:c.419-42del
ENST00000467842.1:n.2640del
NM_001063.3:c.1688-42del	NP_001054.1:n.1688-42del
XM_011513100.1:c.1688-42del	XP_011511402.1:n.1688-42del
NM_001354703.1:c.1556-42del	NP_001341632.1:n.1556-42del
NM_001354704.1:c.1307-42del	NP_001341633.1:n.1307-42del
NM_001063.4:c.1688-42del MANE Select	NP_001054.2:n.1688-42del
NM_001354703.2:c.1556-42del	NP_001341632.2:n.1556-42del
NM_001354704.2:c.1307-42del	NP_001341633.2:n.1307-42del