Canonical Allele Identifier: CA2687076944

Gene: KAT6A

Linked Data

• gnomAD v4: 8-41933184-GGCT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.41933192_41933194del , CM000670.2:g.41933192_41933194del	GRCh38
NC_000008.10:g.41790710_41790712del , CM000670.1:g.41790710_41790712del	GRCh37
NC_000008.9:g.41909867_41909869del	NCBI36
NG_042093.1:g.123840_123842del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265713.8:c.5033_5035del MANE Select	ENSP00000265713.2:p.Gln1678del
ENST00000396930.4:c.5033_5035del	ENSP00000380136.3:p.Gln1678del
ENST00000406337.6:c.5039_5041del	ENSP00000385888.2:p.Gln1680del
ENST00000649817.1:c.3714_3716del
ENST00000265713.6:c.5033_5035del	ENSP00000265713.2:p.Gln1678del
ENST00000396930.3:c.5033_5035del	ENSP00000380136.3:p.Gln1678del
ENST00000406337.5:c.5033_5035del	ENSP00000385888.1:p.Gln1678del
NM_001099412.1:c.5033_5035del	NP_001092882.1:p.Gln1678del
NM_001099413.1:c.5033_5035del	NP_001092883.1:p.Gln1678del
NM_006766.3:c.5033_5035del	NP_006757.2:p.Gln1678del
NM_006766.4:c.5033_5035del	NP_006757.2:p.Gln1678del
XM_011544656.1:c.5165_5167del	XP_011542958.1:p.Gln1722del
XM_011544657.1:c.5165_5167del	XP_011542959.1:p.Gln1722del
XM_011544658.1:c.5165_5167del	XP_011542960.1:p.Gln1722del
XM_011544659.1:c.5144_5146del	XP_011542961.1:p.Gln1715del
XM_011544660.1:c.5051_5053del	XP_011542962.1:p.Gln1684del
XM_011544656.2:c.5165_5167del	XP_011542958.1:p.Gln1722del
XM_011544657.3:c.5165_5167del	XP_011542959.1:p.Gln1722del
XM_011544658.3:c.5165_5167del	XP_011542960.1:p.Gln1722del
XM_011544659.2:c.5144_5146del	XP_011542961.1:p.Gln1715del
XM_017013863.1:c.5033_5035del	XP_016869352.1:p.Gln1678del
XM_017013864.2:c.5033_5035del	XP_016869353.1:p.Gln1678del
XM_024447285.1:c.3605_3607del	XP_024303053.1:p.Gln1202del
NM_006766.5:c.5033_5035del MANE Select	NP_006757.2:p.Gln1678del