Canonical Allele Identifier: CA1053735489

Gene: TF

Linked Data

• dbSNP Id: rs1934358199
• gnomAD v3: 3-133775323-C-T
• gnomAD v4: 3-133775323-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133775323C>T , CM000665.2:g.133775323C>T	GRCh38
NC_000003.11:g.133494167C>T , CM000665.1:g.133494167C>T	GRCh37
NC_000003.10:g.134976857C>T	NCBI36
NG_013080.1:g.34191C>T
NG_013080.2:g.118326C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000402696.9:c.1688-110C>T MANE Select	ENSP00000385834.3:n.1688-110C>T
ENST00000402696.7:c.1688-110C>T	ENSP00000385834.3:n.1688-110C>T
ENST00000461695.1:c.419-110C>T
ENST00000467842.1:n.2572C>T
NM_001063.3:c.1688-110C>T	NP_001054.1:n.1688-110C>T
XM_011513100.1:c.1688-110C>T	XP_011511402.1:n.1688-110C>T
NM_001354703.1:c.1556-110C>T	NP_001341632.1:n.1556-110C>T
NM_001354704.1:c.1307-110C>T	NP_001341633.1:n.1307-110C>T
NM_001063.4:c.1688-110C>T MANE Select	NP_001054.2:n.1688-110C>T
NM_001354703.2:c.1556-110C>T	NP_001341632.2:n.1556-110C>T
NM_001354704.2:c.1307-110C>T	NP_001341633.2:n.1307-110C>T