Canonical Allele Identifier: CA1403125008

Gene: TF

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133777198T= , CM000665.2:g.133777198T=	GRCh38
NC_000003.11:g.133496042T= , CM000665.1:g.133496042T=	GRCh37
NC_000003.10:g.134978732T=	NCBI36
NG_013080.1:g.36066T=
NG_013080.2:g.120201T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.2022T= MANE Select	ENSP00000385834.3:p.Tyr674=
ENST00000402696.7:c.2022T=	ENSP00000385834.3:p.Tyr674=
ENST00000461695.1:c.753T=
ENST00000467842.1:n.3016T=
NM_001063.3:c.2022T=	NP_001054.1:p.Tyr674=
XM_011513100.1:c.2022T=	XP_011511402.1:p.Tyr674=
NM_001354703.1:c.1890T=	NP_001341632.1:p.Tyr630=
NM_001354704.1:c.1641T=	NP_001341633.1:p.Tyr547=
NM_001063.4:c.2022T= MANE Select	NP_001054.2:p.Tyr674=
NM_001354703.2:c.1890T=	NP_001341632.2:p.Tyr630=
NM_001354704.2:c.1641T=	NP_001341633.2:p.Tyr547=