Canonical Allele Identifier: CA354604939

Gene: TF

Linked Data

• MyVariant Identifiers: chr3:g.133475803A>C (hg19) ; chr3:g.133756959A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133756959A>C , CM000665.2:g.133756959A>C	GRCh38
NC_000003.11:g.133475803A>C , CM000665.1:g.133475803A>C	GRCh37
NC_000003.10:g.134958493A>C	NCBI36
NG_013080.1:g.15827A>C
NG_013080.2:g.99962A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.820A>C MANE Select	ENSP00000385834.3:p.Ser274Arg
ENST00000402696.7:c.820A>C	ENSP00000385834.3:p.Ser274Arg
ENST00000485977.1:c.185A>C	ENSP00000418716.1:p.Lys62Thr
NM_001063.3:c.820A>C	NP_001054.1:p.Ser274Arg
XM_011513100.1:c.820A>C	XP_011511402.1:p.Ser274Arg
NM_001354703.1:c.688A>C	NP_001341632.1:p.Ser230Arg
NM_001354704.1:c.439A>C	NP_001341633.1:p.Ser147Arg
NM_001063.4:c.820A>C MANE Select	NP_001054.2:p.Ser274Arg
NM_001354703.2:c.688A>C	NP_001341632.2:p.Ser230Arg
NM_001354704.2:c.439A>C	NP_001341633.2:p.Ser147Arg