Canonical Allele Identifier: CA1779196014

Gene: KAT6A

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.41933677C= , CM000670.2:g.41933677C=	GRCh38
NC_000008.10:g.41791195C= , CM000670.1:g.41791195C=	GRCh37
NC_000008.9:g.41910352C=	NCBI36
NG_042093.1:g.123350G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265713.8:c.4543G= MANE Select	ENSP00000265713.2:p.Glu1515=
ENST00000396930.4:c.4543G=	ENSP00000380136.3:p.Glu1515=
ENST00000406337.6:c.4549G=	ENSP00000385888.2:p.Glu1517=
ENST00000648335.1:c.4543G=	ENSP00000497086.1:p.Glu1515=
ENST00000649817.1:c.3224G=
ENST00000265713.6:c.4543G=	ENSP00000265713.2:p.Glu1515=
ENST00000396930.3:c.4543G=	ENSP00000380136.3:p.Glu1515=
ENST00000406337.5:c.4543G=	ENSP00000385888.1:p.Glu1515=
NM_001099412.1:c.4543G=	NP_001092882.1:p.Glu1515=
NM_001099413.1:c.4543G=	NP_001092883.1:p.Glu1515=
NM_006766.3:c.4543G=	NP_006757.2:p.Glu1515=
NM_006766.4:c.4543G=	NP_006757.2:p.Glu1515=
XM_011544656.1:c.4675G=	XP_011542958.1:p.Glu1559=
XM_011544657.1:c.4675G=	XP_011542959.1:p.Glu1559=
XM_011544658.1:c.4675G=	XP_011542960.1:p.Glu1559=
XM_011544659.1:c.4654G=	XP_011542961.1:p.Glu1552=
XM_011544660.1:c.4561G=	XP_011542962.1:p.Glu1521=
XM_011544656.2:c.4675G=	XP_011542958.1:p.Glu1559=
XM_011544657.3:c.4675G=	XP_011542959.1:p.Glu1559=
XM_011544658.3:c.4675G=	XP_011542960.1:p.Glu1559=
XM_011544659.2:c.4654G=	XP_011542961.1:p.Glu1552=
XM_017013863.1:c.4543G=	XP_016869352.1:p.Glu1515=
XM_017013864.2:c.4543G=	XP_016869353.1:p.Glu1515=
XM_024447285.1:c.3115G=	XP_024303053.1:p.Glu1039=
NM_006766.5:c.4543G= MANE Select	NP_006757.2:p.Glu1515=