Canonical Allele Identifier: CA1403130737

Gene: TF

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133775442C= , CM000665.2:g.133775442C=	GRCh38
NC_000003.11:g.133494286C= , CM000665.1:g.133494286C=	GRCh37
NC_000003.10:g.134976976C=	NCBI36
NG_013080.1:g.34310C=
NG_013080.2:g.118445C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000402696.9:c.1697C= MANE Select	ENSP00000385834.3:p.Pro566=
ENST00000402696.7:c.1697C=	ENSP00000385834.3:p.Pro566=
ENST00000461695.1:c.428C=
ENST00000467842.1:n.2691C=
NM_001063.3:c.1697C=	NP_001054.1:p.Pro566=
XM_011513100.1:c.1697C=	XP_011511402.1:p.Pro566=
NM_001354703.1:c.1565C=	NP_001341632.1:p.Pro522=
NM_001354704.1:c.1316C=	NP_001341633.1:p.Pro439=
NM_001063.4:c.1697C= MANE Select	NP_001054.2:p.Pro566=
NM_001354703.2:c.1565C=	NP_001341632.2:p.Pro522=
NM_001354704.2:c.1316C=	NP_001341633.2:p.Pro439=