Canonical Allele Identifier: CA371065538

Gene: KAT6A

Linked Data

• dbSNP Id: rs1172030267
• gnomAD v2: 8-41791168-T-C
• gnomAD v4: 8-41933650-T-C
• MyVariant Identifiers: chr8:g.41791168T>C (hg19) ; chr8:g.41933650T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.41933650T>C , CM000670.2:g.41933650T>C	GRCh38
NC_000008.10:g.41791168T>C , CM000670.1:g.41791168T>C	GRCh37
NC_000008.9:g.41910325T>C	NCBI36
NG_042093.1:g.123377A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265713.8:c.4570A>G MANE Select	ENSP00000265713.2:p.Met1524Val
ENST00000396930.4:c.4570A>G	ENSP00000380136.3:p.Met1524Val
ENST00000406337.6:c.4576A>G	ENSP00000385888.2:p.Met1526Val
ENST00000648335.1:c.4570A>G	ENSP00000497086.1:p.Met1524Val
ENST00000649817.1:c.3251A>G
ENST00000265713.6:c.4570A>G	ENSP00000265713.2:p.Met1524Val
ENST00000396930.3:c.4570A>G	ENSP00000380136.3:p.Met1524Val
ENST00000406337.5:c.4570A>G	ENSP00000385888.1:p.Met1524Val
NM_001099412.1:c.4570A>G	NP_001092882.1:p.Met1524Val
NM_001099413.1:c.4570A>G	NP_001092883.1:p.Met1524Val
NM_006766.3:c.4570A>G	NP_006757.2:p.Met1524Val
NM_006766.4:c.4570A>G	NP_006757.2:p.Met1524Val
XM_011544656.1:c.4702A>G	XP_011542958.1:p.Met1568Val
XM_011544657.1:c.4702A>G	XP_011542959.1:p.Met1568Val
XM_011544658.1:c.4702A>G	XP_011542960.1:p.Met1568Val
XM_011544659.1:c.4681A>G	XP_011542961.1:p.Met1561Val
XM_011544660.1:c.4588A>G	XP_011542962.1:p.Met1530Val
XM_011544656.2:c.4702A>G	XP_011542958.1:p.Met1568Val
XM_011544657.3:c.4702A>G	XP_011542959.1:p.Met1568Val
XM_011544658.3:c.4702A>G	XP_011542960.1:p.Met1568Val
XM_011544659.2:c.4681A>G	XP_011542961.1:p.Met1561Val
XM_017013863.1:c.4570A>G	XP_016869352.1:p.Met1524Val
XM_017013864.2:c.4570A>G	XP_016869353.1:p.Met1524Val
XM_024447285.1:c.3142A>G	XP_024303053.1:p.Met1048Val
NM_006766.5:c.4570A>G MANE Select	NP_006757.2:p.Met1524Val