Canonical Allele Identifier: CA1403119499

Gene: TF

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133766408_133766411delinsCAAT , CM000665.2:g.133766408_133766411delinsCAAT	GRCh38
NC_000003.11:g.133485252_133485255delinsCAAT , CM000665.1:g.133485252_133485255delinsCAAT	GRCh37
NC_000003.10:g.134967942_134967945delinsCAAT	NCBI36
NG_013080.1:g.25276_25279delinsCAAT
NG_013080.2:g.109411_109414delinsCAAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.1461_1464delinsCAAT MANE Select	ENSP00000385834.3:p.Tyr487=
ENST00000402696.7:c.1461_1464delinsCAAT	ENSP00000385834.3:p.Tyr487=
ENST00000461695.1:c.131_134delinsCAAT
NM_001063.3:c.1461_1464delinsCAAT	NP_001054.1:p.Tyr487=
XM_011513100.1:c.1461_1464delinsCAAT	XP_011511402.1:p.Tyr487=
NM_001354703.1:c.1329_1332delinsCAAT	NP_001341632.1:p.Tyr443=
NM_001354704.1:c.1080_1083delinsCAAT	NP_001341633.1:p.Tyr360=
NM_001063.4:c.1461_1464delinsCAAT MANE Select	NP_001054.2:p.Tyr487=
NM_001354703.2:c.1329_1332delinsCAAT	NP_001341632.2:p.Tyr443=
NM_001354704.2:c.1080_1083delinsCAAT	NP_001341633.2:p.Tyr360=