Canonical Allele Identifier: CA1779195789

Gene: KAT6A

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.41933165A= , CM000670.2:g.41933165A=	GRCh38
NC_000008.10:g.41790683A= , CM000670.1:g.41790683A=	GRCh37
NC_000008.9:g.41909840A=	NCBI36
NG_042093.1:g.123862T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265713.8:c.5055T= MANE Select	ENSP00000265713.2:p.Pro1685=
ENST00000396930.4:c.5055T=	ENSP00000380136.3:p.Pro1685=
ENST00000406337.6:c.5061T=	ENSP00000385888.2:p.Pro1687=
ENST00000649817.1:c.3736T=
ENST00000265713.6:c.5055T=	ENSP00000265713.2:p.Pro1685=
ENST00000396930.3:c.5055T=	ENSP00000380136.3:p.Pro1685=
ENST00000406337.5:c.5055T=	ENSP00000385888.1:p.Pro1685=
NM_001099412.1:c.5055T=	NP_001092882.1:p.Pro1685=
NM_001099413.1:c.5055T=	NP_001092883.1:p.Pro1685=
NM_006766.3:c.5055T=	NP_006757.2:p.Pro1685=
NM_006766.4:c.5055T=	NP_006757.2:p.Pro1685=
XM_011544656.1:c.5187T=	XP_011542958.1:p.Pro1729=
XM_011544657.1:c.5187T=	XP_011542959.1:p.Pro1729=
XM_011544658.1:c.5187T=	XP_011542960.1:p.Pro1729=
XM_011544659.1:c.5166T=	XP_011542961.1:p.Pro1722=
XM_011544660.1:c.5073T=	XP_011542962.1:p.Pro1691=
XM_011544656.2:c.5187T=	XP_011542958.1:p.Pro1729=
XM_011544657.3:c.5187T=	XP_011542959.1:p.Pro1729=
XM_011544658.3:c.5187T=	XP_011542960.1:p.Pro1729=
XM_011544659.2:c.5166T=	XP_011542961.1:p.Pro1722=
XM_017013863.1:c.5055T=	XP_016869352.1:p.Pro1685=
XM_017013864.2:c.5055T=	XP_016869353.1:p.Pro1685=
XM_024447285.1:c.3627T=	XP_024303053.1:p.Pro1209=
NM_006766.5:c.5055T= MANE Select	NP_006757.2:p.Pro1685=