Canonical Allele Identifier: CA354605000

Gene: TF

Linked Data

• MyVariant Identifiers: chr3:g.133475828T>G (hg19) ; chr3:g.133756984T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133756984T>G , CM000665.2:g.133756984T>G	GRCh38
NC_000003.11:g.133475828T>G , CM000665.1:g.133475828T>G	GRCh37
NC_000003.10:g.134958518T>G	NCBI36
NG_013080.1:g.15852T>G
NG_013080.2:g.99987T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.845T>G MANE Select	ENSP00000385834.3:p.Ile282Ser
ENST00000402696.7:c.845T>G	ENSP00000385834.3:p.Ile282Ser
ENST00000485977.1:c.210T>G	ENSP00000418716.1:p.Asp70Glu
NM_001063.3:c.845T>G	NP_001054.1:p.Ile282Ser
XM_011513100.1:c.845T>G	XP_011511402.1:p.Ile282Ser
NM_001354703.1:c.713T>G	NP_001341632.1:p.Ile238Ser
NM_001354704.1:c.464T>G	NP_001341633.1:p.Ile155Ser
NM_001063.4:c.845T>G MANE Select	NP_001054.2:p.Ile282Ser
NM_001354703.2:c.713T>G	NP_001341632.2:p.Ile238Ser
NM_001354704.2:c.464T>G	NP_001341633.2:p.Ile155Ser