Canonical Allele Identifier: CA1403107478

Gene: TF

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133757000C= , CM000665.2:g.133757000C=	GRCh38
NC_000003.11:g.133475844C= , CM000665.1:g.133475844C=	GRCh37
NC_000003.10:g.134958534C=	NCBI36
NG_013080.1:g.15868C=
NG_013080.2:g.100003C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.861C= MANE Select	ENSP00000385834.3:p.Asn287=
ENST00000402696.7:c.861C=	ENSP00000385834.3:p.Asn287=
ENST00000485977.1:c.226C=	ENSP00000418716.1:p.Pro76=
NM_001063.3:c.861C=	NP_001054.1:p.Asn287=
XM_011513100.1:c.861C=	XP_011511402.1:p.Asn287=
NM_001354703.1:c.729C=	NP_001341632.1:p.Asn243=
NM_001354704.1:c.480C=	NP_001341633.1:p.Asn160=
NM_001063.4:c.861C= MANE Select	NP_001054.2:p.Asn287=
NM_001354703.2:c.729C=	NP_001341632.2:p.Asn243=
NM_001354704.2:c.480C=	NP_001341633.2:p.Asn160=