Canonical Allele Identifier: CA1403123371

Gene: TF

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133775874_133775877delinsGTAA , CM000665.2:g.133775874_133775877delinsGTAA	GRCh38
NC_000003.11:g.133494718_133494721delinsGTAA , CM000665.1:g.133494718_133494721delinsGTAA	GRCh37
NC_000003.10:g.134977408_134977411delinsGTAA	NCBI36
NG_013080.1:g.34742_34745delinsGTAA
NG_013080.2:g.118877_118880delinsGTAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.1872+257_1872+260delinsGTAA MANE Select	ENSP00000385834.3:n.1872+257_1872+260delinsGTAA
ENST00000402696.7:c.1872+257_1872+260delinsGTAA	ENSP00000385834.3:n.1872+257_1872+260delinsGTAA
ENST00000461695.1:c.603+257_603+260delinsGTAA
ENST00000467842.1:n.2866+257_2866+260delinsGTAA
NM_001063.3:c.1872+257_1872+260delinsGTAA	NP_001054.1:n.1872+257_1872+260delinsGTAA
XM_011513100.1:c.1872+257_1872+260delinsGTAA	XP_011511402.1:n.1872+257_1872+260delinsGTAA
NM_001354703.1:c.1740+257_1740+260delinsGTAA	NP_001341632.1:n.1740+257_1740+260delinsGTAA
NM_001354704.1:c.1491+257_1491+260delinsGTAA	NP_001341633.1:n.1491+257_1491+260delinsGTAA
NM_001063.4:c.1872+257_1872+260delinsGTAA MANE Select	NP_001054.2:n.1872+257_1872+260delinsGTAA
NM_001354703.2:c.1740+257_1740+260delinsGTAA	NP_001341632.2:n.1740+257_1740+260delinsGTAA
NM_001354704.2:c.1491+257_1491+260delinsGTAA	NP_001341633.2:n.1491+257_1491+260delinsGTAA