Canonical Allele Identifier: CA1403124621

Gene: TF

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133777013C= , CM000665.2:g.133777013C=	GRCh38
NC_000003.11:g.133495857C= , CM000665.1:g.133495857C=	GRCh37
NC_000003.10:g.134978547C=	NCBI36
NG_013080.1:g.35881C=
NG_013080.2:g.120016C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000402696.9:c.1873-36C= MANE Select	ENSP00000385834.3:n.1873-36C=
ENST00000402696.7:c.1873-36C=	ENSP00000385834.3:n.1873-36C=
ENST00000461695.1:c.604-36C=
ENST00000467842.1:n.2867-36C=
NM_001063.3:c.1873-36C=	NP_001054.1:n.1873-36C=
XM_011513100.1:c.1873-36C=	XP_011511402.1:n.1873-36C=
NM_001354703.1:c.1741-36C=	NP_001341632.1:n.1741-36C=
NM_001354704.1:c.1492-36C=	NP_001341633.1:n.1492-36C=
NM_001063.4:c.1873-36C= MANE Select	NP_001054.2:n.1873-36C=
NM_001354703.2:c.1741-36C=	NP_001341632.2:n.1741-36C=
NM_001354704.2:c.1492-36C=	NP_001341633.2:n.1492-36C=