Canonical Allele Identifier: CA354610148

Gene: TF

Linked Data

• MyVariant Identifiers: chr3:g.133494298C>T (hg19) ; chr3:g.133775454C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133775454C>T , CM000665.2:g.133775454C>T	GRCh38
NC_000003.11:g.133494298C>T , CM000665.1:g.133494298C>T	GRCh37
NC_000003.10:g.134976988C>T	NCBI36
NG_013080.1:g.34322C>T
NG_013080.2:g.118457C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.1709C>T MANE Select	ENSP00000385834.3:p.Ala570Val
ENST00000402696.7:c.1709C>T	ENSP00000385834.3:p.Ala570Val
ENST00000461695.1:c.440C>T
ENST00000467842.1:n.2703C>T
NM_001063.3:c.1709C>T	NP_001054.1:p.Ala570Val
XM_011513100.1:c.1709C>T	XP_011511402.1:p.Ala570Val
NM_001354703.1:c.1577C>T	NP_001341632.1:p.Ala526Val
NM_001354704.1:c.1328C>T	NP_001341633.1:p.Ala443Val
NM_001063.4:c.1709C>T MANE Select	NP_001054.2:p.Ala570Val
NM_001354703.2:c.1577C>T	NP_001341632.2:p.Ala526Val
NM_001354704.2:c.1328C>T	NP_001341633.2:p.Ala443Val