Canonical Allele Identifier: CA395669043
Gene: KAT8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.31120424G>T , CM000678.2:g.31120424G>T GRCh38
NC_000016.9:g.31131745G>T , CM000678.1:g.31131745G>T GRCh37
NC_000016.8:g.31039246G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000219797.9:c.372G>T MANE Select ENSP00000219797.3:p.Glu124Asp
ENST00000219797.8:c.372G>T ENSP00000219797.3:p.Glu124Asp
ENST00000448516.6:c.372G>T ENSP00000406037.2:p.Glu124Asp
ENST00000539683.2:n.357G>T
ENST00000543774.6:c.372G>T ENSP00000456933.2:p.Glu124Asp
NM_032188.2:c.372G>T NP_115564.2:p.Glu124Asp
NM_182958.2:c.372G>T NP_892003.2:p.Glu124Asp
XM_011545969.1:c.-103G>T XP_011544271.1:n.-103G>T
XM_011545970.1:c.-103G>T XP_011544272.1:n.-103G>T
XM_011545971.1:c.-103G>T XP_011544273.1:n.-103G>T
NM_032188.3:c.372G>T MANE Select NP_115564.2:p.Glu124Asp
NM_182958.3:c.372G>T NP_892003.2:p.Glu124Asp
NM_182958.4:c.372G>T NP_892003.2:p.Glu124Asp