Canonical Allele Identifier: CA1403125013

Gene: TF

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133777199G= , CM000665.2:g.133777199G=	GRCh38
NC_000003.11:g.133496043G= , CM000665.1:g.133496043G=	GRCh37
NC_000003.10:g.134978733G=	NCBI36
NG_013080.1:g.36067G=
NG_013080.2:g.120202G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.2023G= MANE Select	ENSP00000385834.3:p.Val675=
ENST00000402696.7:c.2023G=	ENSP00000385834.3:p.Val675=
ENST00000461695.1:c.754G=
ENST00000467842.1:n.3017G=
NM_001063.3:c.2023G=	NP_001054.1:p.Val675=
XM_011513100.1:c.2023G=	XP_011511402.1:p.Val675=
NM_001354703.1:c.1891G=	NP_001341632.1:p.Val631=
NM_001354704.1:c.1642G=	NP_001341633.1:p.Val548=
NM_001063.4:c.2023G= MANE Select	NP_001054.2:p.Val675=
NM_001354703.2:c.1891G=	NP_001341632.2:p.Val631=
NM_001354704.2:c.1642G=	NP_001341633.2:p.Val548=