Canonical Allele Identifier: CA354610347
Gene: TF HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.133775507A>C , CM000665.2:g.133775507A>C GRCh38
NC_000003.11:g.133494351A>C , CM000665.1:g.133494351A>C GRCh37
NC_000003.10:g.134977041A>C NCBI36
NG_013080.1:g.34375A>C
NG_013080.2:g.118510A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000402696.9:c.1762A>C MANE Select ENSP00000385834.3:p.Lys588Gln
ENST00000402696.7:c.1762A>C ENSP00000385834.3:p.Lys588Gln
ENST00000461695.1:c.493A>C
ENST00000467842.1:n.2756A>C
NM_001063.3:c.1762A>C NP_001054.1:p.Lys588Gln
XM_011513100.1:c.1762A>C XP_011511402.1:p.Lys588Gln
NM_001354703.1:c.1630A>C NP_001341632.1:p.Lys544Gln
NM_001354704.1:c.1381A>C NP_001341633.1:p.Lys461Gln
NM_001063.4:c.1762A>C MANE Select NP_001054.2:p.Lys588Gln
NM_001354703.2:c.1630A>C NP_001341632.2:p.Lys544Gln
NM_001354704.2:c.1381A>C NP_001341633.2:p.Lys461Gln