Canonical Allele Identifier: CA1053728955

Gene: TF

Linked Data

• dbSNP Id: rs1933862323

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133757208_133757209del , CM000665.2:g.133757208_133757209del	GRCh38
NC_000003.11:g.133476052_133476053del , CM000665.1:g.133476052_133476053del	GRCh37
NC_000003.10:g.134958742_134958743del	NCBI36
NG_013080.1:g.16076_16077del
NG_013080.2:g.100211_100212del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.870+199_870+200del MANE Select	ENSP00000385834.3:n.870+199_870+200del
ENST00000402696.7:c.870+199_870+200del	ENSP00000385834.3:n.870+199_870+200del
ENST00000485977.1:c.235+199_235+200del	ENSP00000418716.1:n.235+199_235+200del
NM_001063.3:c.870+199_870+200del	NP_001054.1:n.870+199_870+200del
XM_011513100.1:c.870+199_870+200del	XP_011511402.1:n.870+199_870+200del
NM_001354703.1:c.738+199_738+200del	NP_001341632.1:n.738+199_738+200del
NM_001354704.1:c.489+199_489+200del	NP_001341633.1:n.489+199_489+200del
NM_001063.4:c.870+199_870+200del MANE Select	NP_001054.2:n.870+199_870+200del
NM_001354703.2:c.738+199_738+200del	NP_001341632.2:n.738+199_738+200del
NM_001354704.2:c.489+199_489+200del	NP_001341633.2:n.489+199_489+200del