Canonical Allele Identifier: CA2758478533
Gene: TF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.133766274del , CM000665.2:g.133766274del GRCh38
NC_000003.11:g.133485118del , CM000665.1:g.133485118del GRCh37
NC_000003.10:g.134967808del NCBI36
NG_013080.1:g.25142del
NG_013080.2:g.109277del

Transcript Alleles

HGVS Amino-acid Change
ENST00000402696.9:c.1331-4del MANE Select ENSP00000385834.3:n.1331-4del
ENST00000402696.7:c.1331-4del ENSP00000385834.3:n.1331-4del
NM_001063.3:c.1331-4del NP_001054.1:n.1331-4del
XM_011513100.1:c.1331-4del XP_011511402.1:n.1331-4del
NM_001354703.1:c.1199-4del NP_001341632.1:n.1199-4del
NM_001354704.1:c.950-4del NP_001341633.1:n.950-4del
NM_001063.4:c.1331-4del MANE Select NP_001054.2:n.1331-4del
NM_001354703.2:c.1199-4del NP_001341632.2:n.1199-4del
NM_001354704.2:c.950-4del NP_001341633.2:n.950-4del