Canonical Allele Identifier: CA2667772163

Gene: TF

Linked Data

• gnomAD v4: 3-133775744-GTGCATTT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133775745_133775751del , CM000665.2:g.133775745_133775751del	GRCh38
NC_000003.11:g.133494589_133494595del , CM000665.1:g.133494589_133494595del	GRCh37
NC_000003.10:g.134977279_134977285del	NCBI36
NG_013080.1:g.34613_34619del
NG_013080.2:g.118748_118754del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.1872+128_1872+134del MANE Select	ENSP00000385834.3:n.1872+128_1872+134del
ENST00000402696.7:c.1872+128_1872+134del	ENSP00000385834.3:n.1872+128_1872+134del
ENST00000461695.1:c.603+128_603+134del
ENST00000467842.1:n.2866+128_2866+134del
NM_001063.3:c.1872+128_1872+134del	NP_001054.1:n.1872+128_1872+134del
XM_011513100.1:c.1872+128_1872+134del	XP_011511402.1:n.1872+128_1872+134del
NM_001354703.1:c.1740+128_1740+134del	NP_001341632.1:n.1740+128_1740+134del
NM_001354704.1:c.1491+128_1491+134del	NP_001341633.1:n.1491+128_1491+134del
NM_001063.4:c.1872+128_1872+134del MANE Select	NP_001054.2:n.1872+128_1872+134del
NM_001354703.2:c.1740+128_1740+134del	NP_001341632.2:n.1740+128_1740+134del
NM_001354704.2:c.1491+128_1491+134del	NP_001341633.2:n.1491+128_1491+134del