Canonical Allele Identifier: CA435815820

Gene: TF

Linked Data

• dbSNP Id: rs1195691077
• gnomAD v2: 3-133494330-C-T
• gnomAD v4: 3-133775486-C-T
• COSMIC: COSM3695826
• MyVariant Identifiers: chr3:g.133494330C>T (hg19) ; chr3:g.133775486C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133775486C>T , CM000665.2:g.133775486C>T	GRCh38
NC_000003.11:g.133494330C>T , CM000665.1:g.133494330C>T	GRCh37
NC_000003.10:g.134977020C>T	NCBI36
NG_013080.1:g.34354C>T
NG_013080.2:g.118489C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.1741C>T MANE Select	ENSP00000385834.3:p.Leu581=
ENST00000402696.7:c.1741C>T	ENSP00000385834.3:p.Leu581=
ENST00000461695.1:c.472C>T
ENST00000467842.1:n.2735C>T
NM_001063.3:c.1741C>T	NP_001054.1:p.Leu581=
XM_011513100.1:c.1741C>T	XP_011511402.1:p.Leu581=
NM_001354703.1:c.1609C>T	NP_001341632.1:p.Leu537=
NM_001354704.1:c.1360C>T	NP_001341633.1:p.Leu454=
NM_001063.4:c.1741C>T MANE Select	NP_001054.2:p.Leu581=
NM_001354703.2:c.1609C>T	NP_001341632.2:p.Leu537=
NM_001354704.2:c.1360C>T	NP_001341633.2:p.Leu454=