Canonical Allele Identifier: CA354610794
Gene: TF HGNC NCBI

Linked Data

dbSNP Id: rs1458924106

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.133777012_133777017del , CM000665.2:g.133777012_133777017del GRCh38
NC_000003.11:g.133495856_133495861del , CM000665.1:g.133495856_133495861del GRCh37
NC_000003.10:g.134978546_134978551del NCBI36
NG_013080.1:g.35880_35885del
NG_013080.2:g.120015_120020del

Transcript Alleles

HGVS Amino-acid change
ENST00000402696.9:c.1873-37_1873-32del MANE Select ENSP00000385834.3:n.1873-37_1873-32del
ENST00000402696.7:c.1873-37_1873-32del ENSP00000385834.3:n.1873-37_1873-32del
ENST00000461695.1:c.604-37_604-32del
ENST00000467842.1:n.2867-37_2867-32del
NM_001063.3:c.1873-37_1873-32del NP_001054.1:n.1873-37_1873-32del
XM_011513100.1:c.1873-37_1873-32del XP_011511402.1:n.1873-37_1873-32del
NM_001354703.1:c.1741-37_1741-32del NP_001341632.1:n.1741-37_1741-32del
NM_001354704.1:c.1492-37_1492-32del NP_001341633.1:n.1492-37_1492-32del
NM_001063.4:c.1873-37_1873-32del MANE Select NP_001054.2:n.1873-37_1873-32del
NM_001354703.2:c.1741-37_1741-32del NP_001341632.2:n.1741-37_1741-32del
NM_001354704.2:c.1492-37_1492-32del NP_001341633.2:n.1492-37_1492-32del