Canonical Allele Identifier: CA2758476178
Gene: TF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.133775438_133775439dup , CM000665.2:g.133775438_133775439dup GRCh38
NC_000003.11:g.133494282_133494283dup , CM000665.1:g.133494282_133494283dup GRCh37
NC_000003.10:g.134976972_134976973dup NCBI36
NG_013080.1:g.34306_34307dup
NG_013080.2:g.118441_118442dup

Transcript Alleles

HGVS Amino-acid change
ENST00000402696.9:c.1693_1694dup MANE Select ENSP00000385834.3:p.Asn565LysfsTer10
ENST00000402696.7:c.1693_1694dup ENSP00000385834.3:p.Asn565LysfsTer10
ENST00000461695.1:c.424_425dup
ENST00000467842.1:n.2687_2688dup
NM_001063.3:c.1693_1694dup NP_001054.1:p.Asn565LysfsTer10
XM_011513100.1:c.1693_1694dup XP_011511402.1:p.Asn565LysfsTer10
NM_001354703.1:c.1561_1562dup NP_001341632.1:p.Asn521LysfsTer10
NM_001354704.1:c.1312_1313dup NP_001341633.1:p.Asn438LysfsTer10
NM_001063.4:c.1693_1694dup MANE Select NP_001054.2:p.Asn565LysfsTer10
NM_001354703.2:c.1561_1562dup NP_001341632.2:p.Asn521LysfsTer10
NM_001354704.2:c.1312_1313dup NP_001341633.2:p.Asn438LysfsTer10