Canonical Allele Identifier: CA371066032

Gene: KAT6A

Linked Data

• gnomAD v4: 8-41933869-C-T
• MyVariant Identifiers: chr8:g.41791387C>T (hg19) ; chr8:g.41933869C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.41933869C>T , CM000670.2:g.41933869C>T	GRCh38
NC_000008.10:g.41791387C>T , CM000670.1:g.41791387C>T	GRCh37
NC_000008.9:g.41910544C>T	NCBI36
NG_042093.1:g.123158G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000265713.8:c.4351G>A MANE Select	ENSP00000265713.2:p.Ala1451Thr
ENST00000396930.4:c.4351G>A	ENSP00000380136.3:p.Ala1451Thr
ENST00000406337.6:c.4357G>A	ENSP00000385888.2:p.Ala1453Thr
ENST00000648335.1:c.4351G>A	ENSP00000497086.1:p.Ala1451Thr
ENST00000649817.1:c.3032G>A
ENST00000265713.6:c.4351G>A	ENSP00000265713.2:p.Ala1451Thr
ENST00000396930.3:c.4351G>A	ENSP00000380136.3:p.Ala1451Thr
ENST00000406337.5:c.4351G>A	ENSP00000385888.1:p.Ala1451Thr
NM_001099412.1:c.4351G>A	NP_001092882.1:p.Ala1451Thr
NM_001099413.1:c.4351G>A	NP_001092883.1:p.Ala1451Thr
NM_006766.3:c.4351G>A	NP_006757.2:p.Ala1451Thr
NM_006766.4:c.4351G>A	NP_006757.2:p.Ala1451Thr
XM_011544656.1:c.4483G>A	XP_011542958.1:p.Ala1495Thr
XM_011544657.1:c.4483G>A	XP_011542959.1:p.Ala1495Thr
XM_011544658.1:c.4483G>A	XP_011542960.1:p.Ala1495Thr
XM_011544659.1:c.4462G>A	XP_011542961.1:p.Ala1488Thr
XM_011544660.1:c.4369G>A	XP_011542962.1:p.Ala1457Thr
XM_011544656.2:c.4483G>A	XP_011542958.1:p.Ala1495Thr
XM_011544657.3:c.4483G>A	XP_011542959.1:p.Ala1495Thr
XM_011544658.3:c.4483G>A	XP_011542960.1:p.Ala1495Thr
XM_011544659.2:c.4462G>A	XP_011542961.1:p.Ala1488Thr
XM_017013863.1:c.4351G>A	XP_016869352.1:p.Ala1451Thr
XM_017013864.2:c.4351G>A	XP_016869353.1:p.Ala1451Thr
XM_024447285.1:c.2923G>A	XP_024303053.1:p.Ala975Thr
NM_006766.5:c.4351G>A MANE Select	NP_006757.2:p.Ala1451Thr