Canonical Allele Identifier: CA395677163

Gene: KAT8

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31130279C>T , CM000678.2:g.31130279C>T	GRCh38
NC_000016.9:g.31141600C>T , CM000678.1:g.31141600C>T	GRCh37
NC_000016.8:g.31049101C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000219797.9:c.925C>T MANE Select	ENSP00000219797.3:p.Pro309Ser
ENST00000219797.8:c.925C>T	ENSP00000219797.3:p.Pro309Ser
ENST00000448516.6:c.925C>T	ENSP00000406037.2:p.Pro309Ser
ENST00000537402.1:c.326C>T
ENST00000538768.2:n.1914C>T
ENST00000543774.6:c.925C>T	ENSP00000456933.2:p.Pro309Ser
NM_032188.2:c.925C>T	NP_115564.2:p.Pro309Ser
NM_182958.2:c.925C>T	NP_892003.2:p.Pro309Ser
XM_011545969.1:c.451C>T	XP_011544271.1:p.Pro151Ser
XM_011545970.1:c.451C>T	XP_011544272.1:p.Pro151Ser
XM_011545971.1:c.451C>T	XP_011544273.1:p.Pro151Ser
NM_032188.3:c.925C>T MANE Select	NP_115564.2:p.Pro309Ser
NM_182958.3:c.925C>T	NP_892003.2:p.Pro309Ser
NM_182958.4:c.925C>T	NP_892003.2:p.Pro309Ser