Canonical Allele Identifier: CA435806302

Gene: TF

Linked Data

• MyVariant Identifiers: chr3:g.133475718T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133756874T>G , CM000665.2:g.133756874T>G	GRCh38
NC_000003.11:g.133475718T>G , CM000665.1:g.133475718T>G	GRCh37
NC_000003.10:g.134958408T>G	NCBI36
NG_013080.1:g.15742T>G
NG_013080.2:g.99877T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000402696.9:c.735T>G MANE Select	ENSP00000385834.3:p.Leu245=
ENST00000402696.7:c.735T>G	ENSP00000385834.3:p.Leu245=
ENST00000482271.5:c.354T>G	ENSP00000419338.1:p.Leu118=
ENST00000485977.1:c.158-58T>G	ENSP00000418716.1:n.158-58T>G
NM_001063.3:c.735T>G	NP_001054.1:p.Leu245=
XM_011513100.1:c.735T>G	XP_011511402.1:p.Leu245=
NM_001354703.1:c.603T>G	NP_001341632.1:p.Leu201=
NM_001354704.1:c.354T>G	NP_001341633.1:p.Leu118=
NM_001063.4:c.735T>G MANE Select	NP_001054.2:p.Leu245=
NM_001354703.2:c.603T>G	NP_001341632.2:p.Leu201=
NM_001354704.2:c.354T>G	NP_001341633.2:p.Leu118=