Canonical Allele Identifier: CA83692586

Gene: TF

Linked Data

• dbSNP Id: rs72563178
• gnomAD v2: 3-133494171-TGGCGAGAA-T
• gnomAD v3: 3-133775327-TGGCGAGAA-T
• gnomAD v4: 3-133775327-TGGCGAGAA-T
• MyVariant Identifiers: chr3:g.133494172_133494179del (hg19) ; chr3:g.133775328_133775335del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133775331_133775338del , CM000665.2:g.133775331_133775338del	GRCh38
NC_000003.11:g.133494175_133494182del , CM000665.1:g.133494175_133494182del	GRCh37
NC_000003.10:g.134976865_134976872del	NCBI36
NG_013080.1:g.34199_34206del
NG_013080.2:g.118334_118341del

Transcript Alleles

HGVS	Amino-acid change
ENST00000402696.9:c.1688-102_1688-95del MANE Select	ENSP00000385834.3:n.1688-102_1688-95del
ENST00000402696.7:c.1688-102_1688-95del	ENSP00000385834.3:n.1688-102_1688-95del
ENST00000461695.1:c.419-102_419-95del
ENST00000467842.1:n.2580_2587del
NM_001063.3:c.1688-102_1688-95del	NP_001054.1:n.1688-102_1688-95del
XM_011513100.1:c.1688-102_1688-95del	XP_011511402.1:n.1688-102_1688-95del
NM_001354703.1:c.1556-102_1556-95del	NP_001341632.1:n.1556-102_1556-95del
NM_001354704.1:c.1307-102_1307-95del	NP_001341633.1:n.1307-102_1307-95del
NM_001063.4:c.1688-102_1688-95del MANE Select	NP_001054.2:n.1688-102_1688-95del
NM_001354703.2:c.1556-102_1556-95del	NP_001341632.2:n.1556-102_1556-95del
NM_001354704.2:c.1307-102_1307-95del	NP_001341633.2:n.1307-102_1307-95del