Canonical Allele Identifier: CA2667764549

Gene: TF

Linked Data

• gnomAD v4: 3-133757110-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133757110A>T , CM000665.2:g.133757110A>T	GRCh38
NC_000003.11:g.133475954A>T , CM000665.1:g.133475954A>T	GRCh37
NC_000003.10:g.134958644A>T	NCBI36
NG_013080.1:g.15978A>T
NG_013080.2:g.100113A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.870+101A>T MANE Select	ENSP00000385834.3:n.870+101A>T
ENST00000402696.7:c.870+101A>T	ENSP00000385834.3:n.870+101A>T
ENST00000485977.1:c.235+101A>T	ENSP00000418716.1:n.235+101A>T
NM_001063.3:c.870+101A>T	NP_001054.1:n.870+101A>T
XM_011513100.1:c.870+101A>T	XP_011511402.1:n.870+101A>T
NM_001354703.1:c.738+101A>T	NP_001341632.1:n.738+101A>T
NM_001354704.1:c.489+101A>T	NP_001341633.1:n.489+101A>T
NM_001063.4:c.870+101A>T MANE Select	NP_001054.2:n.870+101A>T
NM_001354703.2:c.738+101A>T	NP_001341632.2:n.738+101A>T
NM_001354704.2:c.489+101A>T	NP_001341633.2:n.489+101A>T