Canonical Allele Identifier: CA435806688

Gene: TF

Linked Data

• MyVariant Identifiers: chr3:g.133475838T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133756994T>C , CM000665.2:g.133756994T>C	GRCh38
NC_000003.11:g.133475838T>C , CM000665.1:g.133475838T>C	GRCh37
NC_000003.10:g.134958528T>C	NCBI36
NG_013080.1:g.15862T>C
NG_013080.2:g.99997T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.855T>C MANE Select	ENSP00000385834.3:p.Leu285=
ENST00000402696.7:c.855T>C	ENSP00000385834.3:p.Leu285=
ENST00000485977.1:c.220T>C	ENSP00000418716.1:p.Ser74Pro
NM_001063.3:c.855T>C	NP_001054.1:p.Leu285=
XM_011513100.1:c.855T>C	XP_011511402.1:p.Leu285=
NM_001354703.1:c.723T>C	NP_001341632.1:p.Leu241=
NM_001354704.1:c.474T>C	NP_001341633.1:p.Leu158=
NM_001063.4:c.855T>C MANE Select	NP_001054.2:p.Leu285=
NM_001354703.2:c.723T>C	NP_001341632.2:p.Leu241=
NM_001354704.2:c.474T>C	NP_001341633.2:p.Leu158=