Canonical Allele Identifier: CA648502205

Gene: TF

Linked Data

• COSMIC: COSN19366400

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133775247_133775248del , CM000665.2:g.133775247_133775248del	GRCh38
NC_000003.11:g.133494091_133494092del , CM000665.1:g.133494091_133494092del	GRCh37
NC_000003.10:g.134976781_134976782del	NCBI36
NG_013080.1:g.34115_34116del
NG_013080.2:g.118250_118251del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.1688-186_1688-185del MANE Select	ENSP00000385834.3:n.1688-186_1688-185del
ENST00000402696.7:c.1688-186_1688-185del	ENSP00000385834.3:n.1688-186_1688-185del
ENST00000461695.1:c.419-186_419-185del
ENST00000467842.1:n.2496_2497del
NM_001063.3:c.1688-186_1688-185del	NP_001054.1:n.1688-186_1688-185del
XM_011513100.1:c.1688-186_1688-185del	XP_011511402.1:n.1688-186_1688-185del
NM_001354703.1:c.1556-186_1556-185del	NP_001341632.1:n.1556-186_1556-185del
NM_001354704.1:c.1307-186_1307-185del	NP_001341633.1:n.1307-186_1307-185del
NM_001063.4:c.1688-186_1688-185del MANE Select	NP_001054.2:n.1688-186_1688-185del
NM_001354703.2:c.1556-186_1556-185del	NP_001341632.2:n.1556-186_1556-185del
NM_001354704.2:c.1307-186_1307-185del	NP_001341633.2:n.1307-186_1307-185del