Canonical Allele Identifier: CA6926264
Gene: GTF3A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27430555A>C , CM000675.2:g.27430555A>C GRCh38
NC_000013.10:g.28004692A>C , CM000675.1:g.28004692A>C GRCh37
NC_000013.9:g.26902692A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000381140.10:c.422A>C MANE Select ENSP00000370532.5:p.Lys141Thr
ENST00000381140.8:c.422A>C ENSP00000370532.4:p.Lys141Thr
ENST00000419181.5:c.422A>C ENSP00000389655.1:p.Lys141Thr
ENST00000435781.5:c.*12A>C ENSP00000409175.1:n.*12A>C
ENST00000438571.5:c.*334A>C ENSP00000387806.1:n.*334A>C
ENST00000439403.5:c.596A>C ENSP00000393050.2:p.Lys199Thr
ENST00000466776.5:n.309A>C
ENST00000470606.5:n.1152A>C
ENST00000493903.1:n.297A>C
NM_002097.2:c.422A>C NP_002088.2:p.Lys141Thr
NM_002097.3:c.422A>C MANE Select NP_002088.2:p.Lys141Thr