Canonical Allele Identifier: CA4729386

Gene: KAT6A

Linked Data

• ClinVar Variation Id: 1942764
• ClinVar RCV Id: RCV002646965
• dbSNP Id: rs777472787
• ExAC: 8:41790752 C / T
• gnomAD v2: 8-41790752-C-T
• gnomAD v4: 8-41933234-C-T
• MyVariant Identifiers: chr8:g.41790752C>T (hg19) ; chr8:g.41790752_41790773delinsTGGCGGCTGTGGCTGCTGTGGA (hg19) ; chr8:g.41933234C>T (hg38) ; chr8:g.41933234_41933255delinsTGGCGGCTGTGGCTGCTGTGGA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.41933234C>T , CM000670.2:g.41933234C>T	GRCh38
NC_000008.10:g.41790752C>T , CM000670.1:g.41790752C>T	GRCh37
NC_000008.9:g.41909909C>T	NCBI36
NG_042093.1:g.123793G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265713.8:c.4986G>A MANE Select	ENSP00000265713.2:p.Pro1662=
ENST00000396930.4:c.4986G>A	ENSP00000380136.3:p.Pro1662=
ENST00000406337.6:c.4992G>A	ENSP00000385888.2:p.Pro1664=
ENST00000648335.1:c.4986G>A	ENSP00000497086.1:p.Pro1662=
ENST00000649817.1:c.3667G>A
ENST00000265713.6:c.4986G>A	ENSP00000265713.2:p.Pro1662=
ENST00000396930.3:c.4986G>A	ENSP00000380136.3:p.Pro1662=
ENST00000406337.5:c.4986G>A	ENSP00000385888.1:p.Pro1662=
NM_001099412.1:c.4986G>A	NP_001092882.1:p.Pro1662=
NM_001099413.1:c.4986G>A	NP_001092883.1:p.Pro1662=
NM_006766.3:c.4986G>A	NP_006757.2:p.Pro1662=
NM_006766.4:c.4986G>A	NP_006757.2:p.Pro1662=
XM_011544656.1:c.5118G>A	XP_011542958.1:p.Pro1706=
XM_011544657.1:c.5118G>A	XP_011542959.1:p.Pro1706=
XM_011544658.1:c.5118G>A	XP_011542960.1:p.Pro1706=
XM_011544659.1:c.5097G>A	XP_011542961.1:p.Pro1699=
XM_011544660.1:c.5004G>A	XP_011542962.1:p.Pro1668=
XM_011544656.2:c.5118G>A	XP_011542958.1:p.Pro1706=
XM_011544657.3:c.5118G>A	XP_011542959.1:p.Pro1706=
XM_011544658.3:c.5118G>A	XP_011542960.1:p.Pro1706=
XM_011544659.2:c.5097G>A	XP_011542961.1:p.Pro1699=
XM_017013863.1:c.4986G>A	XP_016869352.1:p.Pro1662=
XM_017013864.2:c.4986G>A	XP_016869353.1:p.Pro1662=
XM_024447285.1:c.3558G>A	XP_024303053.1:p.Pro1186=
NM_006766.5:c.4986G>A MANE Select	NP_006757.2:p.Pro1662=