Canonical Allele Identifier: CA2577907321

Gene: TF

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133766233G>A , CM000665.2:g.133766233G>A	GRCh38
NC_000003.11:g.133485077G>A , CM000665.1:g.133485077G>A	GRCh37
NC_000003.10:g.134967767G>A	NCBI36
NG_013080.1:g.25101G>A
NG_013080.2:g.109236G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.1331-45G>A MANE Select	ENSP00000385834.3:n.1331-45G>A
ENST00000402696.7:c.1331-45G>A	ENSP00000385834.3:n.1331-45G>A
NM_001063.3:c.1331-45G>A	NP_001054.1:n.1331-45G>A
XM_011513100.1:c.1331-45G>A	XP_011511402.1:n.1331-45G>A
NM_001354703.1:c.1199-45G>A	NP_001341632.1:n.1199-45G>A
NM_001354704.1:c.950-45G>A	NP_001341633.1:n.950-45G>A
NM_001063.4:c.1331-45G>A MANE Select	NP_001054.2:n.1331-45G>A
NM_001354703.2:c.1199-45G>A	NP_001341632.2:n.1199-45G>A
NM_001354704.2:c.950-45G>A	NP_001341633.2:n.950-45G>A