Canonical Allele Identifier: CA1403130644

Gene: TF

Linked Data

• dbSNP Id: rs1934359027

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133775345del , CM000665.2:g.133775345del	GRCh38
NC_000003.11:g.133494189del , CM000665.1:g.133494189del	GRCh37
NC_000003.10:g.134976879del	NCBI36
NG_013080.1:g.34213del
NG_013080.2:g.118348del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.1688-88del MANE Select	ENSP00000385834.3:n.1688-88del
ENST00000402696.7:c.1688-88del	ENSP00000385834.3:n.1688-88del
ENST00000461695.1:c.419-88del
ENST00000467842.1:n.2594del
NM_001063.3:c.1688-88del	NP_001054.1:n.1688-88del
XM_011513100.1:c.1688-88del	XP_011511402.1:n.1688-88del
NM_001354703.1:c.1556-88del	NP_001341632.1:n.1556-88del
NM_001354704.1:c.1307-88del	NP_001341633.1:n.1307-88del
NM_001063.4:c.1688-88del MANE Select	NP_001054.2:n.1688-88del
NM_001354703.2:c.1556-88del	NP_001341632.2:n.1556-88del
NM_001354704.2:c.1307-88del	NP_001341633.2:n.1307-88del