Canonical Allele Identifier: CA2687076939
Gene: KAT6A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.41933156_41933209del , CM000670.2:g.41933156_41933209del GRCh38
NC_000008.10:g.41790674_41790727del , CM000670.1:g.41790674_41790727del GRCh37
NC_000008.9:g.41909831_41909884del NCBI36
NG_042093.1:g.123829_123882del

Transcript Alleles

HGVS Amino-acid Change
ENST00000265713.8:c.5022_5075del MANE Select ENSP00000265713.2:p.Pro1675_Pro1692del
ENST00000396930.4:c.5022_5075del ENSP00000380136.3:p.Pro1675_Pro1692del
ENST00000406337.6:c.5028_5081del ENSP00000385888.2:p.Pro1677_Pro1694del
ENST00000649817.1:c.3703_3756del
ENST00000265713.6:c.5022_5075del ENSP00000265713.2:p.Pro1675_Pro1692del
ENST00000396930.3:c.5022_5075del ENSP00000380136.3:p.Pro1675_Pro1692del
ENST00000406337.5:c.5022_5075del ENSP00000385888.1:p.Pro1675_Pro1692del
NM_001099412.1:c.5022_5075del NP_001092882.1:p.Pro1675_Pro1692del
NM_001099413.1:c.5022_5075del NP_001092883.1:p.Pro1675_Pro1692del
NM_006766.3:c.5022_5075del NP_006757.2:p.Pro1675_Pro1692del
NM_006766.4:c.5022_5075del NP_006757.2:p.Pro1675_Pro1692del
XM_011544656.1:c.5154_5207del XP_011542958.1:p.Pro1719_Pro1736del
XM_011544657.1:c.5154_5207del XP_011542959.1:p.Pro1719_Pro1736del
XM_011544658.1:c.5154_5207del XP_011542960.1:p.Pro1719_Pro1736del
XM_011544659.1:c.5133_5186del XP_011542961.1:p.Pro1712_Pro1729del
XM_011544660.1:c.5040_5093del XP_011542962.1:p.Pro1681_Pro1698del
XM_011544656.2:c.5154_5207del XP_011542958.1:p.Pro1719_Pro1736del
XM_011544657.3:c.5154_5207del XP_011542959.1:p.Pro1719_Pro1736del
XM_011544658.3:c.5154_5207del XP_011542960.1:p.Pro1719_Pro1736del
XM_011544659.2:c.5133_5186del XP_011542961.1:p.Pro1712_Pro1729del
XM_017013863.1:c.5022_5075del XP_016869352.1:p.Pro1675_Pro1692del
XM_017013864.2:c.5022_5075del XP_016869353.1:p.Pro1675_Pro1692del
XM_024447285.1:c.3594_3647del XP_024303053.1:p.Pro1199_Pro1216del
NM_006766.5:c.5022_5075del MANE Select NP_006757.2:p.Pro1675_Pro1692del