Canonical Allele Identifier: CA354611432

Gene: TF

Linked Data

• gnomAD v4: 3-133777190-G-A
• MyVariant Identifiers: chr3:g.133496034G>A (hg19) ; chr3:g.133777190G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133777190G>A , CM000665.2:g.133777190G>A	GRCh38
NC_000003.11:g.133496034G>A , CM000665.1:g.133496034G>A	GRCh37
NC_000003.10:g.134978724G>A	NCBI36
NG_013080.1:g.36058G>A
NG_013080.2:g.120193G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.2014G>A MANE Select	ENSP00000385834.3:p.Glu672Lys
ENST00000402696.7:c.2014G>A	ENSP00000385834.3:p.Glu672Lys
ENST00000461695.1:c.745G>A
ENST00000467842.1:n.3008G>A
NM_001063.3:c.2014G>A	NP_001054.1:p.Glu672Lys
XM_011513100.1:c.2014G>A	XP_011511402.1:p.Glu672Lys
NM_001354703.1:c.1882G>A	NP_001341632.1:p.Glu628Lys
NM_001354704.1:c.1633G>A	NP_001341633.1:p.Glu545Lys
NM_001063.4:c.2014G>A MANE Select	NP_001054.2:p.Glu672Lys
NM_001354703.2:c.1882G>A	NP_001341632.2:p.Glu628Lys
NM_001354704.2:c.1633G>A	NP_001341633.2:p.Glu545Lys