Canonical Allele Identifier: CA8022146

Gene: KAT8

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31130505A>G , CM000678.2:g.31130505A>G	GRCh38
NC_000016.9:g.31141826A>G , CM000678.1:g.31141826A>G	GRCh37
NC_000016.8:g.31049327A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_032188.3:c.1056A>G MANE Select	NP_115564.2:p.Pro352=
ENST00000219797.9:c.1056A>G MANE Select	ENSP00000219797.3:p.Pro352=
NM_032188.2:c.1056A>G	NP_115564.2:p.Pro352=
NM_182958.2:c.1056A>G	NP_892003.2:p.Pro352=
NM_182958.3:c.1056A>G	NP_892003.2:p.Pro352=
NM_182958.4:c.1056A>G	NP_892003.2:p.Pro352=
ENST00000219797.8:c.1056A>G	ENSP00000219797.3:p.Pro352=
ENST00000448516.6:c.1056A>G	ENSP00000406037.2:p.Pro352=
ENST00000537402.1:c.457A>G
ENST00000538768.2:n.2045A>G
ENST00000543774.6:c.1056A>G	ENSP00000456933.2:p.Pro352=
ENST00000573144.1:n.50A>G
XM_011545969.1:c.582A>G	XP_011544271.1:p.Pro194=
XM_011545970.1:c.582A>G	XP_011544272.1:p.Pro194=
XM_011545971.1:c.582A>G	XP_011544273.1:p.Pro194=