Canonical Allele Identifier: CA1403122730

Gene: TF

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133775511C= , CM000665.2:g.133775511C=	GRCh38
NC_000003.11:g.133494355C= , CM000665.1:g.133494355C=	GRCh37
NC_000003.10:g.134977045C=	NCBI36
NG_013080.1:g.34379C=
NG_013080.2:g.118514C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.1766C= MANE Select	ENSP00000385834.3:p.Pro589=
ENST00000402696.7:c.1766C=	ENSP00000385834.3:p.Pro589=
ENST00000461695.1:c.497C=
ENST00000467842.1:n.2760C=
NM_001063.3:c.1766C=	NP_001054.1:p.Pro589=
XM_011513100.1:c.1766C=	XP_011511402.1:p.Pro589=
NM_001354703.1:c.1634C=	NP_001341632.1:p.Pro545=
NM_001354704.1:c.1385C=	NP_001341633.1:p.Pro462=
NM_001063.4:c.1766C= MANE Select	NP_001054.2:p.Pro589=
NM_001354703.2:c.1634C=	NP_001341632.2:p.Pro545=
NM_001354704.2:c.1385C=	NP_001341633.2:p.Pro462=