Canonical Allele Identifier: CA354604853

Gene: TF

Linked Data

• gnomAD v4: 3-133756914-G-A
• MyVariant Identifiers: chr3:g.133475758G>A (hg19) ; chr3:g.133756914G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133756914G>A , CM000665.2:g.133756914G>A	GRCh38
NC_000003.11:g.133475758G>A , CM000665.1:g.133475758G>A	GRCh37
NC_000003.10:g.134958448G>A	NCBI36
NG_013080.1:g.15782G>A
NG_013080.2:g.99917G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.775G>A MANE Select	ENSP00000385834.3:p.Asp259Asn
ENST00000402696.7:c.775G>A	ENSP00000385834.3:p.Asp259Asn
ENST00000482271.5:c.394G>A	ENSP00000419338.1:p.Asp132Asn
ENST00000485977.1:c.158-18G>A	ENSP00000418716.1:n.158-18G>A
NM_001063.3:c.775G>A	NP_001054.1:p.Asp259Asn
XM_011513100.1:c.775G>A	XP_011511402.1:p.Asp259Asn
NM_001354703.1:c.643G>A	NP_001341632.1:p.Asp215Asn
NM_001354704.1:c.394G>A	NP_001341633.1:p.Asp132Asn
NM_001063.4:c.775G>A MANE Select	NP_001054.2:p.Asp259Asn
NM_001354703.2:c.643G>A	NP_001341632.2:p.Asp215Asn
NM_001354704.2:c.394G>A	NP_001341633.2:p.Asp132Asn