Canonical Allele Identifier: CA354605027

Gene: TF

Linked Data

• gnomAD v4: 3-133756996-T-G
• MyVariant Identifiers: chr3:g.133475840T>G (hg19) ; chr3:g.133756996T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133756996T>G , CM000665.2:g.133756996T>G	GRCh38
NC_000003.11:g.133475840T>G , CM000665.1:g.133475840T>G	GRCh37
NC_000003.10:g.134958530T>G	NCBI36
NG_013080.1:g.15864T>G
NG_013080.2:g.99999T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.857T>G MANE Select	ENSP00000385834.3:p.Leu286Arg
ENST00000402696.7:c.857T>G	ENSP00000385834.3:p.Leu286Arg
ENST00000485977.1:c.222T>G	ENSP00000418716.1:p.Ser74=
NM_001063.3:c.857T>G	NP_001054.1:p.Leu286Arg
XM_011513100.1:c.857T>G	XP_011511402.1:p.Leu286Arg
NM_001354703.1:c.725T>G	NP_001341632.1:p.Leu242Arg
NM_001354704.1:c.476T>G	NP_001341633.1:p.Leu159Arg
NM_001063.4:c.857T>G MANE Select	NP_001054.2:p.Leu286Arg
NM_001354703.2:c.725T>G	NP_001341632.2:p.Leu242Arg
NM_001354704.2:c.476T>G	NP_001341633.2:p.Leu159Arg