Canonical Allele Identifier: CA1403124917

Gene: TF

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133777150C= , CM000665.2:g.133777150C=	GRCh38
NC_000003.11:g.133495994C= , CM000665.1:g.133495994C=	GRCh37
NC_000003.10:g.134978684C=	NCBI36
NG_013080.1:g.36018C=
NG_013080.2:g.120153C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.1974C= MANE Select	ENSP00000385834.3:p.Ala658=
ENST00000402696.7:c.1974C=	ENSP00000385834.3:p.Ala658=
ENST00000461695.1:c.705C=
ENST00000467842.1:n.2968C=
NM_001063.3:c.1974C=	NP_001054.1:p.Ala658=
XM_011513100.1:c.1974C=	XP_011511402.1:p.Ala658=
NM_001354703.1:c.1842C=	NP_001341632.1:p.Ala614=
NM_001354704.1:c.1593C=	NP_001341633.1:p.Ala531=
NM_001063.4:c.1974C= MANE Select	NP_001054.2:p.Ala658=
NM_001354703.2:c.1842C=	NP_001341632.2:p.Ala614=
NM_001354704.2:c.1593C=	NP_001341633.2:p.Ala531=