Canonical Allele Identifier: CA1053735462

Gene: TF

Linked Data

• dbSNP Id: rs1934354754
• gnomAD v3: 3-133775187-C-T
• gnomAD v4: 3-133775187-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133775187C>T , CM000665.2:g.133775187C>T	GRCh38
NC_000003.11:g.133494031C>T , CM000665.1:g.133494031C>T	GRCh37
NC_000003.10:g.134976721C>T	NCBI36
NG_013080.1:g.34055C>T
NG_013080.2:g.118190C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.1688-246C>T MANE Select	ENSP00000385834.3:n.1688-246C>T
ENST00000402696.7:c.1688-246C>T	ENSP00000385834.3:n.1688-246C>T
ENST00000461695.1:c.419-246C>T
ENST00000467842.1:n.2436C>T
NM_001063.3:c.1688-246C>T	NP_001054.1:n.1688-246C>T
XM_011513100.1:c.1688-246C>T	XP_011511402.1:n.1688-246C>T
NM_001354703.1:c.1556-246C>T	NP_001341632.1:n.1556-246C>T
NM_001354704.1:c.1307-246C>T	NP_001341633.1:n.1307-246C>T
NM_001063.4:c.1688-246C>T MANE Select	NP_001054.2:n.1688-246C>T
NM_001354703.2:c.1556-246C>T	NP_001341632.2:n.1556-246C>T
NM_001354704.2:c.1307-246C>T	NP_001341633.2:n.1307-246C>T