Canonical Allele Identifier: CA354610074

Gene: TF

Linked Data

• dbSNP Id: rs1335254709
• gnomAD v2: 3-133494283-A-T
• gnomAD v4: 3-133775439-A-T
• MyVariant Identifiers: chr3:g.133494283A>T (hg19) ; chr3:g.133775439A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133775439A>T , CM000665.2:g.133775439A>T	GRCh38
NC_000003.11:g.133494283A>T , CM000665.1:g.133494283A>T	GRCh37
NC_000003.10:g.134976973A>T	NCBI36
NG_013080.1:g.34307A>T
NG_013080.2:g.118442A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.1694A>T MANE Select	ENSP00000385834.3:p.Asn565Ile
ENST00000402696.7:c.1694A>T	ENSP00000385834.3:p.Asn565Ile
ENST00000461695.1:c.425A>T
ENST00000467842.1:n.2688A>T
NM_001063.3:c.1694A>T	NP_001054.1:p.Asn565Ile
XM_011513100.1:c.1694A>T	XP_011511402.1:p.Asn565Ile
NM_001354703.1:c.1562A>T	NP_001341632.1:p.Asn521Ile
NM_001354704.1:c.1313A>T	NP_001341633.1:p.Asn438Ile
NM_001063.4:c.1694A>T MANE Select	NP_001054.2:p.Asn565Ile
NM_001354703.2:c.1562A>T	NP_001341632.2:p.Asn521Ile
NM_001354704.2:c.1313A>T	NP_001341633.2:p.Asn438Ile