Canonical Allele Identifier: CA1403107493

Gene: TF

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133757012_133757013delinsAT , CM000665.2:g.133757012_133757013delinsAT	GRCh38
NC_000003.11:g.133475856_133475857delinsAT , CM000665.1:g.133475856_133475857delinsAT	GRCh37
NC_000003.10:g.134958546_134958547delinsAT	NCBI36
NG_013080.1:g.15880_15881delinsAT
NG_013080.2:g.100015_100016delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.870+3_870+4delinsAT MANE Select	ENSP00000385834.3:n.870+3_870+4delinsAT
ENST00000402696.7:c.870+3_870+4delinsAT	ENSP00000385834.3:n.870+3_870+4delinsAT
ENST00000485977.1:c.235+3_235+4delinsAT	ENSP00000418716.1:n.235+3_235+4delinsAT
NM_001063.3:c.870+3_870+4delinsAT	NP_001054.1:n.870+3_870+4delinsAT
XM_011513100.1:c.870+3_870+4delinsAT	XP_011511402.1:n.870+3_870+4delinsAT
NM_001354703.1:c.738+3_738+4delinsAT	NP_001341632.1:n.738+3_738+4delinsAT
NM_001354704.1:c.489+3_489+4delinsAT	NP_001341633.1:n.489+3_489+4delinsAT
NM_001063.4:c.870+3_870+4delinsAT MANE Select	NP_001054.2:n.870+3_870+4delinsAT
NM_001354703.2:c.738+3_738+4delinsAT	NP_001341632.2:n.738+3_738+4delinsAT
NM_001354704.2:c.489+3_489+4delinsAT	NP_001341633.2:n.489+3_489+4delinsAT