Canonical Allele Identifier: CA1403130655

Gene: TF

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133775364C= , CM000665.2:g.133775364C=	GRCh38
NC_000003.11:g.133494208C= , CM000665.1:g.133494208C=	GRCh37
NC_000003.10:g.134976898C=	NCBI36
NG_013080.1:g.34232C=
NG_013080.2:g.118367C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.1688-69C= MANE Select	ENSP00000385834.3:n.1688-69C=
ENST00000402696.7:c.1688-69C=	ENSP00000385834.3:n.1688-69C=
ENST00000461695.1:c.419-69C=
ENST00000467842.1:n.2613C=
NM_001063.3:c.1688-69C=	NP_001054.1:n.1688-69C=
XM_011513100.1:c.1688-69C=	XP_011511402.1:n.1688-69C=
NM_001354703.1:c.1556-69C=	NP_001341632.1:n.1556-69C=
NM_001354704.1:c.1307-69C=	NP_001341633.1:n.1307-69C=
NM_001063.4:c.1688-69C= MANE Select	NP_001054.2:n.1688-69C=
NM_001354703.2:c.1556-69C=	NP_001341632.2:n.1556-69C=
NM_001354704.2:c.1307-69C=	NP_001341633.2:n.1307-69C=