Canonical Allele Identifier: CA354610280

Gene: TF

Linked Data

• MyVariant Identifiers: chr3:g.133494325A>C (hg19) ; chr3:g.133775481A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133775481A>C , CM000665.2:g.133775481A>C	GRCh38
NC_000003.11:g.133494325A>C , CM000665.1:g.133494325A>C	GRCh37
NC_000003.10:g.134977015A>C	NCBI36
NG_013080.1:g.34349A>C
NG_013080.2:g.118484A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.1736A>C MANE Select	ENSP00000385834.3:p.Glu579Ala
ENST00000402696.7:c.1736A>C	ENSP00000385834.3:p.Glu579Ala
ENST00000461695.1:c.467A>C
ENST00000467842.1:n.2730A>C
NM_001063.3:c.1736A>C	NP_001054.1:p.Glu579Ala
XM_011513100.1:c.1736A>C	XP_011511402.1:p.Glu579Ala
NM_001354703.1:c.1604A>C	NP_001341632.1:p.Glu535Ala
NM_001354704.1:c.1355A>C	NP_001341633.1:p.Glu452Ala
NM_001063.4:c.1736A>C MANE Select	NP_001054.2:p.Glu579Ala
NM_001354703.2:c.1604A>C	NP_001341632.2:p.Glu535Ala
NM_001354704.2:c.1355A>C	NP_001341633.2:p.Glu452Ala