Canonical Allele Identifier: CA395674316

Gene: KAT8

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31128137A>G , CM000678.2:g.31128137A>G	GRCh38
NC_000016.9:g.31139458A>G , CM000678.1:g.31139458A>G	GRCh37
NC_000016.8:g.31046959A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000219797.9:c.769A>G MANE Select	ENSP00000219797.3:p.Lys257Glu
ENST00000219797.8:c.769A>G	ENSP00000219797.3:p.Lys257Glu
ENST00000448516.6:c.769A>G	ENSP00000406037.2:p.Lys257Glu
ENST00000537402.1:c.170A>G
ENST00000538768.2:n.1758A>G
ENST00000543774.6:c.769A>G	ENSP00000456933.2:p.Lys257Glu
NM_032188.2:c.769A>G	NP_115564.2:p.Lys257Glu
NM_182958.2:c.769A>G	NP_892003.2:p.Lys257Glu
XM_011545969.1:c.295A>G	XP_011544271.1:p.Lys99Glu
XM_011545970.1:c.295A>G	XP_011544272.1:p.Lys99Glu
XM_011545971.1:c.295A>G	XP_011544273.1:p.Lys99Glu
NM_032188.3:c.769A>G MANE Select	NP_115564.2:p.Lys257Glu
NM_182958.3:c.769A>G	NP_892003.2:p.Lys257Glu
NM_182958.4:c.769A>G	NP_892003.2:p.Lys257Glu