Canonical Allele Identifier: CA1403107729

Gene: TF

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133757206_133757208delinsCCG , CM000665.2:g.133757206_133757208delinsCCG	GRCh38
NC_000003.11:g.133476050_133476052delinsCCG , CM000665.1:g.133476050_133476052delinsCCG	GRCh37
NC_000003.10:g.134958740_134958742delinsCCG	NCBI36
NG_013080.1:g.16074_16076delinsCCG
NG_013080.2:g.100209_100211delinsCCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.870+197_870+199delinsCCG MANE Select	ENSP00000385834.3:n.870+197_870+199delinsCCG
ENST00000402696.7:c.870+197_870+199delinsCCG	ENSP00000385834.3:n.870+197_870+199delinsCCG
ENST00000485977.1:c.235+197_235+199delinsCCG	ENSP00000418716.1:n.235+197_235+199delinsCCG
NM_001063.3:c.870+197_870+199delinsCCG	NP_001054.1:n.870+197_870+199delinsCCG
XM_011513100.1:c.870+197_870+199delinsCCG	XP_011511402.1:n.870+197_870+199delinsCCG
NM_001354703.1:c.738+197_738+199delinsCCG	NP_001341632.1:n.738+197_738+199delinsCCG
NM_001354704.1:c.489+197_489+199delinsCCG	NP_001341633.1:n.489+197_489+199delinsCCG
NM_001063.4:c.870+197_870+199delinsCCG MANE Select	NP_001054.2:n.870+197_870+199delinsCCG
NM_001354703.2:c.738+197_738+199delinsCCG	NP_001341632.2:n.738+197_738+199delinsCCG
NM_001354704.2:c.489+197_489+199delinsCCG	NP_001341633.2:n.489+197_489+199delinsCCG