Canonical Allele Identifier: CA371064474

Gene: KAT6A

Linked Data

• MyVariant Identifiers: chr8:g.41790880G>C (hg19) ; chr8:g.41933362G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.41933362G>C , CM000670.2:g.41933362G>C	GRCh38
NC_000008.10:g.41790880G>C , CM000670.1:g.41790880G>C	GRCh37
NC_000008.9:g.41910037G>C	NCBI36
NG_042093.1:g.123665C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265713.8:c.4858C>G MANE Select	ENSP00000265713.2:p.Gln1620Glu
ENST00000396930.4:c.4858C>G	ENSP00000380136.3:p.Gln1620Glu
ENST00000406337.6:c.4864C>G	ENSP00000385888.2:p.Gln1622Glu
ENST00000648335.1:c.4858C>G	ENSP00000497086.1:p.Gln1620Glu
ENST00000649817.1:c.3539C>G
ENST00000265713.6:c.4858C>G	ENSP00000265713.2:p.Gln1620Glu
ENST00000396930.3:c.4858C>G	ENSP00000380136.3:p.Gln1620Glu
ENST00000406337.5:c.4858C>G	ENSP00000385888.1:p.Gln1620Glu
NM_001099412.1:c.4858C>G	NP_001092882.1:p.Gln1620Glu
NM_001099413.1:c.4858C>G	NP_001092883.1:p.Gln1620Glu
NM_006766.3:c.4858C>G	NP_006757.2:p.Gln1620Glu
NM_006766.4:c.4858C>G	NP_006757.2:p.Gln1620Glu
XM_011544656.1:c.4990C>G	XP_011542958.1:p.Gln1664Glu
XM_011544657.1:c.4990C>G	XP_011542959.1:p.Gln1664Glu
XM_011544658.1:c.4990C>G	XP_011542960.1:p.Gln1664Glu
XM_011544659.1:c.4969C>G	XP_011542961.1:p.Gln1657Glu
XM_011544660.1:c.4876C>G	XP_011542962.1:p.Gln1626Glu
XM_011544656.2:c.4990C>G	XP_011542958.1:p.Gln1664Glu
XM_011544657.3:c.4990C>G	XP_011542959.1:p.Gln1664Glu
XM_011544658.3:c.4990C>G	XP_011542960.1:p.Gln1664Glu
XM_011544659.2:c.4969C>G	XP_011542961.1:p.Gln1657Glu
XM_017013863.1:c.4858C>G	XP_016869352.1:p.Gln1620Glu
XM_017013864.2:c.4858C>G	XP_016869353.1:p.Gln1620Glu
XM_024447285.1:c.3430C>G	XP_024303053.1:p.Gln1144Glu
NM_006766.5:c.4858C>G MANE Select	NP_006757.2:p.Gln1620Glu