Canonical Allele Identifier: CA435806699

Gene: TF

Linked Data

• MyVariant Identifiers: chr3:g.133475850C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133757006C>A , CM000665.2:g.133757006C>A	GRCh38
NC_000003.11:g.133475850C>A , CM000665.1:g.133475850C>A	GRCh37
NC_000003.10:g.134958540C>A	NCBI36
NG_013080.1:g.15874C>A
NG_013080.2:g.100009C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.867C>A MANE Select	ENSP00000385834.3:p.Ala289=
ENST00000402696.7:c.867C>A	ENSP00000385834.3:p.Ala289=
ENST00000485977.1:c.232C>A	ENSP00000418716.1:p.Pro78Thr
NM_001063.3:c.867C>A	NP_001054.1:p.Ala289=
XM_011513100.1:c.867C>A	XP_011511402.1:p.Ala289=
NM_001354703.1:c.735C>A	NP_001341632.1:p.Ala245=
NM_001354704.1:c.486C>A	NP_001341633.1:p.Ala162=
NM_001063.4:c.867C>A MANE Select	NP_001054.2:p.Ala289=
NM_001354703.2:c.735C>A	NP_001341632.2:p.Ala245=
NM_001354704.2:c.486C>A	NP_001341633.2:p.Ala162=