Canonical Allele Identifier: CA354604974
Gene: TF HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.133756974G>C , CM000665.2:g.133756974G>C GRCh38
NC_000003.11:g.133475818G>C , CM000665.1:g.133475818G>C GRCh37
NC_000003.10:g.134958508G>C NCBI36
NG_013080.1:g.15842G>C
NG_013080.2:g.99977G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000402696.9:c.835G>C MANE Select ENSP00000385834.3:p.Glu279Gln
ENST00000402696.7:c.835G>C ENSP00000385834.3:p.Glu279Gln
ENST00000485977.1:c.200G>C ENSP00000418716.1:p.Gly67Ala
NM_001063.3:c.835G>C NP_001054.1:p.Glu279Gln
XM_011513100.1:c.835G>C XP_011511402.1:p.Glu279Gln
NM_001354703.1:c.703G>C NP_001341632.1:p.Glu235Gln
NM_001354704.1:c.454G>C NP_001341633.1:p.Glu152Gln
NM_001063.4:c.835G>C MANE Select NP_001054.2:p.Glu279Gln
NM_001354703.2:c.703G>C NP_001341632.2:p.Glu235Gln
NM_001354704.2:c.454G>C NP_001341633.2:p.Glu152Gln