Canonical Allele Identifier: CA899131367

Gene: TF

Linked Data

• dbSNP Id: rs1229499614
• gnomAD v4: 3-133775378-CA-C
• MyVariant Identifiers: chr3:g.133494223del (hg19) ; chr3:g.133775379del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133775379del , CM000665.2:g.133775379del	GRCh38
NC_000003.11:g.133494223del , CM000665.1:g.133494223del	GRCh37
NC_000003.10:g.134976913del	NCBI36
NG_013080.1:g.34247del
NG_013080.2:g.118382del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.1688-54del MANE Select	ENSP00000385834.3:n.1688-54del
ENST00000402696.7:c.1688-54del	ENSP00000385834.3:n.1688-54del
ENST00000461695.1:c.419-54del
ENST00000467842.1:n.2628del
NM_001063.3:c.1688-54del	NP_001054.1:n.1688-54del
XM_011513100.1:c.1688-54del	XP_011511402.1:n.1688-54del
NM_001354703.1:c.1556-54del	NP_001341632.1:n.1556-54del
NM_001354704.1:c.1307-54del	NP_001341633.1:n.1307-54del
NM_001063.4:c.1688-54del MANE Select	NP_001054.2:n.1688-54del
NM_001354703.2:c.1556-54del	NP_001341632.2:n.1556-54del
NM_001354704.2:c.1307-54del	NP_001341633.2:n.1307-54del