Canonical Allele Identifier: CA2667768508

Gene: TF

Linked Data

• gnomAD v4: 3-133766360-GGCA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133766362_133766364del , CM000665.2:g.133766362_133766364del	GRCh38
NC_000003.11:g.133485206_133485208del , CM000665.1:g.133485206_133485208del	GRCh37
NC_000003.10:g.134967896_134967898del	NCBI36
NG_013080.1:g.25230_25232del
NG_013080.2:g.109365_109367del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.1415_1417del MANE Select	ENSP00000385834.3:p.Ala472del
ENST00000402696.7:c.1415_1417del	ENSP00000385834.3:p.Ala472del
ENST00000461695.1:c.85_87del
NM_001063.3:c.1415_1417del	NP_001054.1:p.Ala472del
XM_011513100.1:c.1415_1417del	XP_011511402.1:p.Ala472del
NM_001354703.1:c.1283_1285del	NP_001341632.1:p.Ala428del
NM_001354704.1:c.1034_1036del	NP_001341633.1:p.Ala345del
NM_001063.4:c.1415_1417del MANE Select	NP_001054.2:p.Ala472del
NM_001354703.2:c.1283_1285del	NP_001341632.2:p.Ala428del
NM_001354704.2:c.1034_1036del	NP_001341633.2:p.Ala345del