Canonical Allele Identifier: CA435815651

Gene: TF

Linked Data

• MyVariant Identifiers: chr3:g.133485234C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133766390C>A , CM000665.2:g.133766390C>A	GRCh38
NC_000003.11:g.133485234C>A , CM000665.1:g.133485234C>A	GRCh37
NC_000003.10:g.134967924C>A	NCBI36
NG_013080.1:g.25258C>A
NG_013080.2:g.109393C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000402696.9:c.1443C>A MANE Select	ENSP00000385834.3:p.Ile481=
ENST00000402696.7:c.1443C>A	ENSP00000385834.3:p.Ile481=
ENST00000461695.1:c.113C>A
NM_001063.3:c.1443C>A	NP_001054.1:p.Ile481=
XM_011513100.1:c.1443C>A	XP_011511402.1:p.Ile481=
NM_001354703.1:c.1311C>A	NP_001341632.1:p.Ile437=
NM_001354704.1:c.1062C>A	NP_001341633.1:p.Ile354=
NM_001063.4:c.1443C>A MANE Select	NP_001054.2:p.Ile481=
NM_001354703.2:c.1311C>A	NP_001341632.2:p.Ile437=
NM_001354704.2:c.1062C>A	NP_001341633.2:p.Ile354=