Canonical Allele Identifier: CA371064312
Gene: KAT6A HGNC NCBI

Linked Data

gnomAD v4: 8-41933320-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.41933320A>G , CM000670.2:g.41933320A>G GRCh38
NC_000008.10:g.41790838A>G , CM000670.1:g.41790838A>G GRCh37
NC_000008.9:g.41909995A>G NCBI36
NG_042093.1:g.123707T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000265713.8:c.4900T>C MANE Select ENSP00000265713.2:p.Ser1634Pro
ENST00000396930.4:c.4900T>C ENSP00000380136.3:p.Ser1634Pro
ENST00000406337.6:c.4906T>C ENSP00000385888.2:p.Ser1636Pro
ENST00000648335.1:c.4900T>C ENSP00000497086.1:p.Ser1634Pro
ENST00000649817.1:c.3581T>C
ENST00000265713.6:c.4900T>C ENSP00000265713.2:p.Ser1634Pro
ENST00000396930.3:c.4900T>C ENSP00000380136.3:p.Ser1634Pro
ENST00000406337.5:c.4900T>C ENSP00000385888.1:p.Ser1634Pro
NM_001099412.1:c.4900T>C NP_001092882.1:p.Ser1634Pro
NM_001099413.1:c.4900T>C NP_001092883.1:p.Ser1634Pro
NM_006766.3:c.4900T>C NP_006757.2:p.Ser1634Pro
NM_006766.4:c.4900T>C NP_006757.2:p.Ser1634Pro
XM_011544656.1:c.5032T>C XP_011542958.1:p.Ser1678Pro
XM_011544657.1:c.5032T>C XP_011542959.1:p.Ser1678Pro
XM_011544658.1:c.5032T>C XP_011542960.1:p.Ser1678Pro
XM_011544659.1:c.5011T>C XP_011542961.1:p.Ser1671Pro
XM_011544660.1:c.4918T>C XP_011542962.1:p.Ser1640Pro
XM_011544656.2:c.5032T>C XP_011542958.1:p.Ser1678Pro
XM_011544657.3:c.5032T>C XP_011542959.1:p.Ser1678Pro
XM_011544658.3:c.5032T>C XP_011542960.1:p.Ser1678Pro
XM_011544659.2:c.5011T>C XP_011542961.1:p.Ser1671Pro
XM_017013863.1:c.4900T>C XP_016869352.1:p.Ser1634Pro
XM_017013864.2:c.4900T>C XP_016869353.1:p.Ser1634Pro
XM_024447285.1:c.3472T>C XP_024303053.1:p.Ser1158Pro
NM_006766.5:c.4900T>C MANE Select NP_006757.2:p.Ser1634Pro