Canonical Allele Identifier: CA918709270

Gene: KAT6B

Linked Data

• dbSNP Id: rs869035066

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.75022173del , CM000672.2:g.75022173del	GRCh38
NC_000010.10:g.76781931del , CM000672.1:g.76781931del	GRCh37
NC_000010.9:g.76451937del	NCBI36
NG_032048.1:g.200761del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000287239.10:c.3314del MANE Select	ENSP00000287239.4:p.Asn1105IlefsTer9
ENST00000372711.2:c.2765del	ENSP00000361796.1:p.Asn922IlefsTer9
ENST00000372714.6:c.2438del	ENSP00000361799.1:p.Asn813IlefsTer9
ENST00000372724.6:c.2765del	ENSP00000361809.2:p.Asn922IlefsTer9
ENST00000372725.6:c.2438del	ENSP00000361810.1:p.Asn813IlefsTer9
ENST00000648048.1:c.3314del	ENSP00000497325.1:p.Asn1105IlefsTer9
ENST00000648370.1:c.2765del	ENSP00000497804.1:p.Asn922IlefsTer9
ENST00000648725.1:c.3314del	ENSP00000497841.1:p.Asn1105IlefsTer9
ENST00000648793.1:n.3792del
ENST00000648892.1:c.2438del	ENSP00000497048.1:p.Asn813IlefsTer9
ENST00000649006.1:c.2438del	ENSP00000498139.1:p.Asn813IlefsTer9
ENST00000649305.1:n.1629del
ENST00000649375.1:c.2765del	ENSP00000498141.1:p.Asn922IlefsTer9
ENST00000649463.1:c.3314del	ENSP00000497166.1:p.Asn1105IlefsTer9
ENST00000650232.1:c.2249del	ENSP00000497570.1:p.Asn750IlefsTer9
ENST00000650610.1:n.2359del
ENST00000287239.8:c.3314del	ENSP00000287239.4:p.Asn1105IlefsTer9
ENST00000372711.1:c.2765del	ENSP00000361796.1:p.Asn922IlefsTer9
ENST00000372714.5:c.2438del	ENSP00000361799.1:p.Asn813IlefsTer9
ENST00000372724.5:c.2438del	ENSP00000361809.1:p.Asn813IlefsTer9
ENST00000372725.5:c.2438del	ENSP00000361810.1:p.Asn813IlefsTer9
ENST00000490365.1:n.5267del
NM_001256468.1:c.2765del	NP_001243397.1:p.Asn922IlefsTer9
NM_001256469.1:c.2438del	NP_001243398.1:p.Asn813IlefsTer9
NM_012330.3:c.3314del	NP_036462.2:p.Asn1105IlefsTer9
XM_005269664.2:c.3314del	XP_005269721.1:p.Asn1105IlefsTer9
XM_017016000.2:c.3314del	XP_016871489.1:p.Asn1105IlefsTer9
XM_017016002.1:c.3314del	XP_016871491.1:p.Asn1105IlefsTer9
XM_017016003.1:c.3314del	XP_016871492.1:p.Asn1105IlefsTer9
XM_017016004.2:c.3152del	XP_016871493.1:p.Asn1051IlefsTer9
XM_017016005.2:c.2765del	XP_016871494.1:p.Asn922IlefsTer9
XM_017016006.2:c.2438del	XP_016871495.1:p.Asn813IlefsTer9
XM_017016008.2:c.2438del	XP_016871497.1:p.Asn813IlefsTer9
XM_017016009.1:c.2276del	XP_016871498.1:p.Asn759IlefsTer9
NM_012330.4:c.3314del MANE Select	NP_036462.2:p.Asn1105IlefsTer9
NM_001370132.1:c.2276del	NP_001357061.1:p.Asn759IlefsTer9
NM_001370133.1:c.1625del	NP_001357062.1:p.Asn542IlefsTer9
NM_001370134.1:c.1229del	NP_001357063.1:p.Asn410IlefsTer9
NM_001370135.1:c.971del	NP_001357064.1:p.Asn324IlefsTer9
NM_001370136.1:c.3314del	NP_001357065.1:p.Asn1105IlefsTer9
NM_001370137.1:c.3314del	NP_001357066.1:p.Asn1105IlefsTer9
NM_001370138.1:c.2765del	NP_001357067.1:p.Asn922IlefsTer9
NM_001370139.1:c.2438del	NP_001357068.1:p.Asn813IlefsTer9
NM_001370140.1:c.2438del	NP_001357069.1:p.Asn813IlefsTer9
NM_001370141.1:c.2438del	NP_001357070.1:p.Asn813IlefsTer9
NM_001370142.1:c.2438del	NP_001357071.1:p.Asn813IlefsTer9
NM_001370143.1:c.2249del	NP_001357072.1:p.Asn750IlefsTer9
NM_001370144.1:c.2249del	NP_001357073.1:p.Asn750IlefsTer9
NM_001256468.2:c.2765del	NP_001243397.1:p.Asn922IlefsTer9
NM_001256469.2:c.2438del	NP_001243398.1:p.Asn813IlefsTer9