Canonical Allele Identifier: CA1403119373
Gene: TF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.133766348G= , CM000665.2:g.133766348G= GRCh38
NC_000003.11:g.133485192G= , CM000665.1:g.133485192G= GRCh37
NC_000003.10:g.134967882G= NCBI36
NG_013080.1:g.25216G=
NG_013080.2:g.109351G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000402696.9:c.1401G= MANE Select ENSP00000385834.3:p.Lys467=
ENST00000402696.7:c.1401G= ENSP00000385834.3:p.Lys467=
ENST00000461695.1:c.71G=
NM_001063.3:c.1401G= NP_001054.1:p.Lys467=
XM_011513100.1:c.1401G= XP_011511402.1:p.Lys467=
NM_001354703.1:c.1269G= NP_001341632.1:p.Lys423=
NM_001354704.1:c.1020G= NP_001341633.1:p.Lys340=
NM_001063.4:c.1401G= MANE Select NP_001054.2:p.Lys467=
NM_001354703.2:c.1269G= NP_001341632.2:p.Lys423=
NM_001354704.2:c.1020G= NP_001341633.2:p.Lys340=