Canonical Allele Identifier: CA899131920

Gene: TF

Linked Data

• dbSNP Id: rs1215990217
• MyVariant Identifiers: chr3:g.133494719_133494721del (hg19) ; chr3:g.133775875_133775877del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133775883_133775885del , CM000665.2:g.133775883_133775885del	GRCh38
NC_000003.11:g.133494727_133494729del , CM000665.1:g.133494727_133494729del	GRCh37
NC_000003.10:g.134977417_134977419del	NCBI36
NG_013080.1:g.34751_34753del
NG_013080.2:g.118886_118888del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.1872+266_1872+268del MANE Select	ENSP00000385834.3:n.1872+266_1872+268del
ENST00000402696.7:c.1872+266_1872+268del	ENSP00000385834.3:n.1872+266_1872+268del
ENST00000461695.1:c.603+266_603+268del
ENST00000467842.1:n.2866+266_2866+268del
NM_001063.3:c.1872+266_1872+268del	NP_001054.1:n.1872+266_1872+268del
XM_011513100.1:c.1872+266_1872+268del	XP_011511402.1:n.1872+266_1872+268del
NM_001354703.1:c.1740+266_1740+268del	NP_001341632.1:n.1740+266_1740+268del
NM_001354704.1:c.1491+266_1491+268del	NP_001341633.1:n.1491+266_1491+268del
NM_001063.4:c.1872+266_1872+268del MANE Select	NP_001054.2:n.1872+266_1872+268del
NM_001354703.2:c.1740+266_1740+268del	NP_001341632.2:n.1740+266_1740+268del
NM_001354704.2:c.1491+266_1491+268del	NP_001341633.2:n.1491+266_1491+268del