Canonical Allele Identifier: CA1779195842

Gene: KAT6A

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.41933243_41933267delinsTGGCTGCTGTGGAGGCGGTGGTGGC , CM000670.2:g.41933243_41933267delinsTGGCTGCTGTGGAGGCGGTGGTGGC	GRCh38
NC_000008.10:g.41790761_41790785delinsTGGCTGCTGTGGAGGCGGTGGTGGC , CM000670.1:g.41790761_41790785delinsTGGCTGCTGTGGAGGCGGTGGTGGC	GRCh37
NC_000008.9:g.41909918_41909942delinsTGGCTGCTGTGGAGGCGGTGGTGGC	NCBI36
NG_042093.1:g.123760_123784delinsGCCACCACCGCCTCCACAGCAGCCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265713.8:c.4953_4977delinsGCCACCACCGCCTCCACAGCAGCCA MANE Select	ENSP00000265713.2:p.Pro1651=
ENST00000396930.4:c.4953_4977delinsGCCACCACCGCCTCCACAGCAGCCA	ENSP00000380136.3:p.Pro1651=
ENST00000406337.6:c.4959_4983delinsGCCACCACCGCCTCCACAGCAGCCA	ENSP00000385888.2:p.Pro1653=
ENST00000648335.1:c.4953_4977delinsGCCACCACCGCCTCCACAGCAGCCA	ENSP00000497086.1:p.Pro1651=
ENST00000649817.1:c.3634_3658delinsGCCACCACCGCCTCCACAGCAGCCA
ENST00000265713.6:c.4953_4977delinsGCCACCACCGCCTCCACAGCAGCCA	ENSP00000265713.2:p.Pro1651=
ENST00000396930.3:c.4953_4977delinsGCCACCACCGCCTCCACAGCAGCCA	ENSP00000380136.3:p.Pro1651=
ENST00000406337.5:c.4953_4977delinsGCCACCACCGCCTCCACAGCAGCCA	ENSP00000385888.1:p.Pro1651=
NM_001099412.1:c.4953_4977delinsGCCACCACCGCCTCCACAGCAGCCA	NP_001092882.1:p.Pro1651=
NM_001099413.1:c.4953_4977delinsGCCACCACCGCCTCCACAGCAGCCA	NP_001092883.1:p.Pro1651=
NM_006766.3:c.4953_4977delinsGCCACCACCGCCTCCACAGCAGCCA	NP_006757.2:p.Pro1651=
NM_006766.4:c.4953_4977delinsGCCACCACCGCCTCCACAGCAGCCA	NP_006757.2:p.Pro1651=
XM_011544656.1:c.5085_5109delinsGCCACCACCGCCTCCACAGCAGCCA	XP_011542958.1:p.Pro1695=
XM_011544657.1:c.5085_5109delinsGCCACCACCGCCTCCACAGCAGCCA	XP_011542959.1:p.Pro1695=
XM_011544658.1:c.5085_5109delinsGCCACCACCGCCTCCACAGCAGCCA	XP_011542960.1:p.Pro1695=
XM_011544659.1:c.5064_5088delinsGCCACCACCGCCTCCACAGCAGCCA	XP_011542961.1:p.Pro1688=
XM_011544660.1:c.4971_4995delinsGCCACCACCGCCTCCACAGCAGCCA	XP_011542962.1:p.Pro1657=
XM_011544656.2:c.5085_5109delinsGCCACCACCGCCTCCACAGCAGCCA	XP_011542958.1:p.Pro1695=
XM_011544657.3:c.5085_5109delinsGCCACCACCGCCTCCACAGCAGCCA	XP_011542959.1:p.Pro1695=
XM_011544658.3:c.5085_5109delinsGCCACCACCGCCTCCACAGCAGCCA	XP_011542960.1:p.Pro1695=
XM_011544659.2:c.5064_5088delinsGCCACCACCGCCTCCACAGCAGCCA	XP_011542961.1:p.Pro1688=
XM_017013863.1:c.4953_4977delinsGCCACCACCGCCTCCACAGCAGCCA	XP_016869352.1:p.Pro1651=
XM_017013864.2:c.4953_4977delinsGCCACCACCGCCTCCACAGCAGCCA	XP_016869353.1:p.Pro1651=
XM_024447285.1:c.3525_3549delinsGCCACCACCGCCTCCACAGCAGCCA	XP_024303053.1:p.Pro1175=
NM_006766.5:c.4953_4977delinsGCCACCACCGCCTCCACAGCAGCCA MANE Select	NP_006757.2:p.Pro1651=