Canonical Allele Identifier: CA354608796

Gene: TF

Linked Data

• dbSNP Id: rs1486415911
• gnomAD v2: 3-133485255-T-A
• gnomAD v3: 3-133766411-T-A
• gnomAD v4: 3-133766411-T-A
• MyVariant Identifiers: chr3:g.133485255T>A (hg19) ; chr3:g.133766411T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133766411T>A , CM000665.2:g.133766411T>A	GRCh38
NC_000003.11:g.133485255T>A , CM000665.1:g.133485255T>A	GRCh37
NC_000003.10:g.134967945T>A	NCBI36
NG_013080.1:g.25279T>A
NG_013080.2:g.109414T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.1464T>A MANE Select	ENSP00000385834.3:p.Asn488Lys
ENST00000402696.7:c.1464T>A	ENSP00000385834.3:p.Asn488Lys
ENST00000461695.1:c.134T>A
NM_001063.3:c.1464T>A	NP_001054.1:p.Asn488Lys
XM_011513100.1:c.1464T>A	XP_011511402.1:p.Asn488Lys
NM_001354703.1:c.1332T>A	NP_001341632.1:p.Asn444Lys
NM_001354704.1:c.1083T>A	NP_001341633.1:p.Asn361Lys
NM_001063.4:c.1464T>A MANE Select	NP_001054.2:p.Asn488Lys
NM_001354703.2:c.1332T>A	NP_001341632.2:p.Asn444Lys
NM_001354704.2:c.1083T>A	NP_001341633.2:p.Asn361Lys