Canonical Allele Identifier: CA1403124873

Gene: TF

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133777121C= , CM000665.2:g.133777121C=	GRCh38
NC_000003.11:g.133495965C= , CM000665.1:g.133495965C=	GRCh37
NC_000003.10:g.134978655C=	NCBI36
NG_013080.1:g.35989C=
NG_013080.2:g.120124C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000402696.9:c.1945C= MANE Select	ENSP00000385834.3:p.Leu649=
ENST00000402696.7:c.1945C=	ENSP00000385834.3:p.Leu649=
ENST00000461695.1:c.676C=
ENST00000467842.1:n.2939C=
NM_001063.3:c.1945C=	NP_001054.1:p.Leu649=
XM_011513100.1:c.1945C=	XP_011511402.1:p.Leu649=
NM_001354703.1:c.1813C=	NP_001341632.1:p.Leu605=
NM_001354704.1:c.1564C=	NP_001341633.1:p.Leu522=
NM_001063.4:c.1945C= MANE Select	NP_001054.2:p.Leu649=
NM_001354703.2:c.1813C=	NP_001341632.2:p.Leu605=
NM_001354704.2:c.1564C=	NP_001341633.2:p.Leu522=