Canonical Allele Identifier: CA354610176

Gene: TF

Linked Data

• gnomAD v4: 3-133775460-A-G
• MyVariant Identifiers: chr3:g.133494304A>G (hg19) ; chr3:g.133775460A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133775460A>G , CM000665.2:g.133775460A>G	GRCh38
NC_000003.11:g.133494304A>G , CM000665.1:g.133494304A>G	GRCh37
NC_000003.10:g.134976994A>G	NCBI36
NG_013080.1:g.34328A>G
NG_013080.2:g.118463A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.1715A>G MANE Select	ENSP00000385834.3:p.Asn572Ser
ENST00000402696.7:c.1715A>G	ENSP00000385834.3:p.Asn572Ser
ENST00000461695.1:c.446A>G
ENST00000467842.1:n.2709A>G
NM_001063.3:c.1715A>G	NP_001054.1:p.Asn572Ser
XM_011513100.1:c.1715A>G	XP_011511402.1:p.Asn572Ser
NM_001354703.1:c.1583A>G	NP_001341632.1:p.Asn528Ser
NM_001354704.1:c.1334A>G	NP_001341633.1:p.Asn445Ser
NM_001063.4:c.1715A>G MANE Select	NP_001054.2:p.Asn572Ser
NM_001354703.2:c.1583A>G	NP_001341632.2:p.Asn528Ser
NM_001354704.2:c.1334A>G	NP_001341633.2:p.Asn445Ser