Canonical Allele Identifier: CA1779196073

Gene: KAT6A

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.41933795A= , CM000670.2:g.41933795A=	GRCh38
NC_000008.10:g.41791313A= , CM000670.1:g.41791313A=	GRCh37
NC_000008.9:g.41910470A=	NCBI36
NG_042093.1:g.123232T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265713.8:c.4425T= MANE Select	ENSP00000265713.2:p.His1475=
ENST00000396930.4:c.4425T=	ENSP00000380136.3:p.His1475=
ENST00000406337.6:c.4431T=	ENSP00000385888.2:p.His1477=
ENST00000648335.1:c.4425T=	ENSP00000497086.1:p.His1475=
ENST00000649817.1:c.3106T=
ENST00000265713.6:c.4425T=	ENSP00000265713.2:p.His1475=
ENST00000396930.3:c.4425T=	ENSP00000380136.3:p.His1475=
ENST00000406337.5:c.4425T=	ENSP00000385888.1:p.His1475=
NM_001099412.1:c.4425T=	NP_001092882.1:p.His1475=
NM_001099413.1:c.4425T=	NP_001092883.1:p.His1475=
NM_006766.3:c.4425T=	NP_006757.2:p.His1475=
NM_006766.4:c.4425T=	NP_006757.2:p.His1475=
XM_011544656.1:c.4557T=	XP_011542958.1:p.His1519=
XM_011544657.1:c.4557T=	XP_011542959.1:p.His1519=
XM_011544658.1:c.4557T=	XP_011542960.1:p.His1519=
XM_011544659.1:c.4536T=	XP_011542961.1:p.His1512=
XM_011544660.1:c.4443T=	XP_011542962.1:p.His1481=
XM_011544656.2:c.4557T=	XP_011542958.1:p.His1519=
XM_011544657.3:c.4557T=	XP_011542959.1:p.His1519=
XM_011544658.3:c.4557T=	XP_011542960.1:p.His1519=
XM_011544659.2:c.4536T=	XP_011542961.1:p.His1512=
XM_017013863.1:c.4425T=	XP_016869352.1:p.His1475=
XM_017013864.2:c.4425T=	XP_016869353.1:p.His1475=
XM_024447285.1:c.2997T=	XP_024303053.1:p.His999=
NM_006766.5:c.4425T= MANE Select	NP_006757.2:p.His1475=