Canonical Allele Identifier: CA395665590

Gene: KAT8

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31117778G>C , CM000678.2:g.31117778G>C	GRCh38
NC_000016.9:g.31129099G>C , CM000678.1:g.31129099G>C	GRCh37
NC_000016.8:g.31036600G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000219797.9:c.97G>C MANE Select	ENSP00000219797.3:p.Gly33Arg
ENST00000652764.1:c.97G>C	ENSP00000498566.1:p.Gly33Arg
ENST00000219797.8:c.97G>C	ENSP00000219797.3:p.Gly33Arg
ENST00000448516.6:c.97G>C	ENSP00000406037.2:p.Gly33Arg
ENST00000539683.2:n.82G>C
ENST00000543774.6:c.97G>C	ENSP00000456933.2:p.Gly33Arg
NM_032188.2:c.97G>C	NP_115564.2:p.Gly33Arg
NM_182958.2:c.97G>C	NP_892003.2:p.Gly33Arg
NM_032188.3:c.97G>C MANE Select	NP_115564.2:p.Gly33Arg
NM_182958.3:c.97G>C	NP_892003.2:p.Gly33Arg
NM_182958.4:c.97G>C	NP_892003.2:p.Gly33Arg