Canonical Allele Identifier: CA371065758

Gene: KAT6A

Linked Data

• MyVariant Identifiers: chr8:g.41791273G>C (hg19) ; chr8:g.41933755G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.41933755G>C , CM000670.2:g.41933755G>C	GRCh38
NC_000008.10:g.41791273G>C , CM000670.1:g.41791273G>C	GRCh37
NC_000008.9:g.41910430G>C	NCBI36
NG_042093.1:g.123272C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265713.8:c.4465C>G MANE Select	ENSP00000265713.2:p.His1489Asp
ENST00000396930.4:c.4465C>G	ENSP00000380136.3:p.His1489Asp
ENST00000406337.6:c.4471C>G	ENSP00000385888.2:p.His1491Asp
ENST00000648335.1:c.4465C>G	ENSP00000497086.1:p.His1489Asp
ENST00000649817.1:c.3146C>G
ENST00000265713.6:c.4465C>G	ENSP00000265713.2:p.His1489Asp
ENST00000396930.3:c.4465C>G	ENSP00000380136.3:p.His1489Asp
ENST00000406337.5:c.4465C>G	ENSP00000385888.1:p.His1489Asp
NM_001099412.1:c.4465C>G	NP_001092882.1:p.His1489Asp
NM_001099413.1:c.4465C>G	NP_001092883.1:p.His1489Asp
NM_006766.3:c.4465C>G	NP_006757.2:p.His1489Asp
NM_006766.4:c.4465C>G	NP_006757.2:p.His1489Asp
XM_011544656.1:c.4597C>G	XP_011542958.1:p.His1533Asp
XM_011544657.1:c.4597C>G	XP_011542959.1:p.His1533Asp
XM_011544658.1:c.4597C>G	XP_011542960.1:p.His1533Asp
XM_011544659.1:c.4576C>G	XP_011542961.1:p.His1526Asp
XM_011544660.1:c.4483C>G	XP_011542962.1:p.His1495Asp
XM_011544656.2:c.4597C>G	XP_011542958.1:p.His1533Asp
XM_011544657.3:c.4597C>G	XP_011542959.1:p.His1533Asp
XM_011544658.3:c.4597C>G	XP_011542960.1:p.His1533Asp
XM_011544659.2:c.4576C>G	XP_011542961.1:p.His1526Asp
XM_017013863.1:c.4465C>G	XP_016869352.1:p.His1489Asp
XM_017013864.2:c.4465C>G	XP_016869353.1:p.His1489Asp
XM_024447285.1:c.3037C>G	XP_024303053.1:p.His1013Asp
NM_006766.5:c.4465C>G MANE Select	NP_006757.2:p.His1489Asp