Canonical Allele Identifier: CA918248396

Gene: KAT6A

Linked Data

• dbSNP Id: rs1564004451

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.41933735_41933737dup , CM000670.2:g.41933735_41933737dup	GRCh38
NC_000008.10:g.41791253_41791255dup , CM000670.1:g.41791253_41791255dup	GRCh37
NC_000008.9:g.41910410_41910412dup	NCBI36
NG_042093.1:g.123290_123292dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265713.8:c.4483_4485dup MANE Select	ENSP00000265713.2:p.Arg1495_Ser1496insArg
ENST00000396930.4:c.4483_4485dup	ENSP00000380136.3:p.Arg1495_Ser1496insArg
ENST00000406337.6:c.4489_4491dup	ENSP00000385888.2:p.Arg1497_Ser1498insArg
ENST00000648335.1:c.4483_4485dup	ENSP00000497086.1:p.Arg1495_Ser1496insArg
ENST00000649817.1:c.3164_3166dup
ENST00000265713.6:c.4483_4485dup	ENSP00000265713.2:p.Arg1495_Ser1496insArg
ENST00000396930.3:c.4483_4485dup	ENSP00000380136.3:p.Arg1495_Ser1496insArg
ENST00000406337.5:c.4483_4485dup	ENSP00000385888.1:p.Arg1495_Ser1496insArg
NM_001099412.1:c.4483_4485dup	NP_001092882.1:p.Arg1495_Ser1496insArg
NM_001099413.1:c.4483_4485dup	NP_001092883.1:p.Arg1495_Ser1496insArg
NM_006766.3:c.4483_4485dup	NP_006757.2:p.Arg1495_Ser1496insArg
NM_006766.4:c.4483_4485dup	NP_006757.2:p.Arg1495_Ser1496insArg
XM_011544656.1:c.4615_4617dup	XP_011542958.1:p.Arg1539_Ser1540insArg
XM_011544657.1:c.4615_4617dup	XP_011542959.1:p.Arg1539_Ser1540insArg
XM_011544658.1:c.4615_4617dup	XP_011542960.1:p.Arg1539_Ser1540insArg
XM_011544659.1:c.4594_4596dup	XP_011542961.1:p.Arg1532_Ser1533insArg
XM_011544660.1:c.4501_4503dup	XP_011542962.1:p.Arg1501_Ser1502insArg
XM_011544656.2:c.4615_4617dup	XP_011542958.1:p.Arg1539_Ser1540insArg
XM_011544657.3:c.4615_4617dup	XP_011542959.1:p.Arg1539_Ser1540insArg
XM_011544658.3:c.4615_4617dup	XP_011542960.1:p.Arg1539_Ser1540insArg
XM_011544659.2:c.4594_4596dup	XP_011542961.1:p.Arg1532_Ser1533insArg
XM_017013863.1:c.4483_4485dup	XP_016869352.1:p.Arg1495_Ser1496insArg
XM_017013864.2:c.4483_4485dup	XP_016869353.1:p.Arg1495_Ser1496insArg
XM_024447285.1:c.3055_3057dup	XP_024303053.1:p.Arg1019_Ser1020insArg
NM_006766.5:c.4483_4485dup MANE Select	NP_006757.2:p.Arg1495_Ser1496insArg