Canonical Allele Identifier: CA2667772259

Gene: TF

Linked Data

• gnomAD v4: 3-133777024-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133777024C>A , CM000665.2:g.133777024C>A	GRCh38
NC_000003.11:g.133495868C>A , CM000665.1:g.133495868C>A	GRCh37
NC_000003.10:g.134978558C>A	NCBI36
NG_013080.1:g.35892C>A
NG_013080.2:g.120027C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000402696.9:c.1873-25C>A MANE Select	ENSP00000385834.3:n.1873-25C>A
ENST00000402696.7:c.1873-25C>A	ENSP00000385834.3:n.1873-25C>A
ENST00000461695.1:c.604-25C>A
ENST00000467842.1:n.2867-25C>A
NM_001063.3:c.1873-25C>A	NP_001054.1:n.1873-25C>A
XM_011513100.1:c.1873-25C>A	XP_011511402.1:n.1873-25C>A
NM_001354703.1:c.1741-25C>A	NP_001341632.1:n.1741-25C>A
NM_001354704.1:c.1492-25C>A	NP_001341633.1:n.1492-25C>A
NM_001063.4:c.1873-25C>A MANE Select	NP_001054.2:n.1873-25C>A
NM_001354703.2:c.1741-25C>A	NP_001341632.2:n.1741-25C>A
NM_001354704.2:c.1492-25C>A	NP_001341633.2:n.1492-25C>A