Canonical Allele Identifier: CA1779196111

Gene: KAT6A

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.41933870A= , CM000670.2:g.41933870A=	GRCh38
NC_000008.10:g.41791388A= , CM000670.1:g.41791388A=	GRCh37
NC_000008.9:g.41910545A=	NCBI36
NG_042093.1:g.123157T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000265713.8:c.4350T= MANE Select	ENSP00000265713.2:p.Leu1450=
ENST00000396930.4:c.4350T=	ENSP00000380136.3:p.Leu1450=
ENST00000406337.6:c.4356T=	ENSP00000385888.2:p.Leu1452=
ENST00000648335.1:c.4350T=	ENSP00000497086.1:p.Leu1450=
ENST00000649817.1:c.3031T=
ENST00000265713.6:c.4350T=	ENSP00000265713.2:p.Leu1450=
ENST00000396930.3:c.4350T=	ENSP00000380136.3:p.Leu1450=
ENST00000406337.5:c.4350T=	ENSP00000385888.1:p.Leu1450=
NM_001099412.1:c.4350T=	NP_001092882.1:p.Leu1450=
NM_001099413.1:c.4350T=	NP_001092883.1:p.Leu1450=
NM_006766.3:c.4350T=	NP_006757.2:p.Leu1450=
NM_006766.4:c.4350T=	NP_006757.2:p.Leu1450=
XM_011544656.1:c.4482T=	XP_011542958.1:p.Leu1494=
XM_011544657.1:c.4482T=	XP_011542959.1:p.Leu1494=
XM_011544658.1:c.4482T=	XP_011542960.1:p.Leu1494=
XM_011544659.1:c.4461T=	XP_011542961.1:p.Leu1487=
XM_011544660.1:c.4368T=	XP_011542962.1:p.Leu1456=
XM_011544656.2:c.4482T=	XP_011542958.1:p.Leu1494=
XM_011544657.3:c.4482T=	XP_011542959.1:p.Leu1494=
XM_011544658.3:c.4482T=	XP_011542960.1:p.Leu1494=
XM_011544659.2:c.4461T=	XP_011542961.1:p.Leu1487=
XM_017013863.1:c.4350T=	XP_016869352.1:p.Leu1450=
XM_017013864.2:c.4350T=	XP_016869353.1:p.Leu1450=
XM_024447285.1:c.2922T=	XP_024303053.1:p.Leu974=
NM_006766.5:c.4350T= MANE Select	NP_006757.2:p.Leu1450=