Canonical Allele Identifier: CA2577907333

Gene: TF

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133766474C>A , CM000665.2:g.133766474C>A	GRCh38
NC_000003.11:g.133485318C>A , CM000665.1:g.133485318C>A	GRCh37
NC_000003.10:g.134968008C>A	NCBI36
NG_013080.1:g.25342C>A
NG_013080.2:g.109477C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.1486+41C>A MANE Select	ENSP00000385834.3:n.1486+41C>A
ENST00000402696.7:c.1486+41C>A	ENSP00000385834.3:n.1486+41C>A
ENST00000461695.1:c.156+41C>A
NM_001063.3:c.1486+41C>A	NP_001054.1:n.1486+41C>A
XM_011513100.1:c.1486+41C>A	XP_011511402.1:n.1486+41C>A
NM_001354703.1:c.1354+41C>A	NP_001341632.1:n.1354+41C>A
NM_001354704.1:c.1105+41C>A	NP_001341633.1:n.1105+41C>A
NM_001063.4:c.1486+41C>A MANE Select	NP_001054.2:n.1486+41C>A
NM_001354703.2:c.1354+41C>A	NP_001341632.2:n.1354+41C>A
NM_001354704.2:c.1105+41C>A	NP_001341633.2:n.1105+41C>A