Canonical Allele Identifier: CA1779195992

Gene: KAT6A

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.41933622A= , CM000670.2:g.41933622A=	GRCh38
NC_000008.10:g.41791140A= , CM000670.1:g.41791140A=	GRCh37
NC_000008.9:g.41910297A=	NCBI36
NG_042093.1:g.123405T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265713.8:c.4598T= MANE Select	ENSP00000265713.2:p.Met1533=
ENST00000396930.4:c.4598T=	ENSP00000380136.3:p.Met1533=
ENST00000406337.6:c.4604T=	ENSP00000385888.2:p.Met1535=
ENST00000648335.1:c.4598T=	ENSP00000497086.1:p.Met1533=
ENST00000649817.1:c.3279T=
ENST00000265713.6:c.4598T=	ENSP00000265713.2:p.Met1533=
ENST00000396930.3:c.4598T=	ENSP00000380136.3:p.Met1533=
ENST00000406337.5:c.4598T=	ENSP00000385888.1:p.Met1533=
NM_001099412.1:c.4598T=	NP_001092882.1:p.Met1533=
NM_001099413.1:c.4598T=	NP_001092883.1:p.Met1533=
NM_006766.3:c.4598T=	NP_006757.2:p.Met1533=
NM_006766.4:c.4598T=	NP_006757.2:p.Met1533=
XM_011544656.1:c.4730T=	XP_011542958.1:p.Met1577=
XM_011544657.1:c.4730T=	XP_011542959.1:p.Met1577=
XM_011544658.1:c.4730T=	XP_011542960.1:p.Met1577=
XM_011544659.1:c.4709T=	XP_011542961.1:p.Met1570=
XM_011544660.1:c.4616T=	XP_011542962.1:p.Met1539=
XM_011544656.2:c.4730T=	XP_011542958.1:p.Met1577=
XM_011544657.3:c.4730T=	XP_011542959.1:p.Met1577=
XM_011544658.3:c.4730T=	XP_011542960.1:p.Met1577=
XM_011544659.2:c.4709T=	XP_011542961.1:p.Met1570=
XM_017013863.1:c.4598T=	XP_016869352.1:p.Met1533=
XM_017013864.2:c.4598T=	XP_016869353.1:p.Met1533=
XM_024447285.1:c.3170T=	XP_024303053.1:p.Met1057=
NM_006766.5:c.4598T= MANE Select	NP_006757.2:p.Met1533=