Canonical Allele Identifier: CA2333794576

Gene: KMT2B

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35732954_35732955delinsAC , CM000681.2:g.35732954_35732955delinsAC	GRCh38
NC_000019.9:g.36223855_36223856delinsAC , CM000681.1:g.36223855_36223856delinsAC	GRCh37
NC_000019.8:g.40915695_40915696delinsAC	NCBI36
NG_052906.1:g.19936_19937delinsAC

Transcript Alleles

HGVS	Amino-acid change
ENST00000592092.2:n.711_712delinsAC
ENST00000673918.2:c.6339_6340delinsAC	ENSP00000501283.1:p.Ser2113=
ENST00000674114.2:c.3946_3947delinsAC	ENSP00000501039.2:n.3946_3947delinsAC
ENST00000684977.1:c.1623_1624delinsAC	ENSP00000509384.1:p.Ser541=
ENST00000689544.1:n.1558_1559delinsAC
ENST00000691421.1:c.1626_1627delinsAC	ENSP00000508674.1:p.Ser542=
ENST00000691855.1:c.5947_5948delinsAC
ENST00000692961.1:c.6405_6406delinsAC	ENSP00000509289.1:p.Ser2135=
ENST00000693677.1:c.704+625_704+626delinsAC	ENSP00000509779.1:n.704+625_704+626delins...
ENST00000420124.4:c.6405_6406delinsAC MANE Select	ENSP00000398837.2:p.Ser2135=
ENST00000673918.1:c.6339_6340delinsAC	ENSP00000501283.1:p.Ser2113=
ENST00000674114.1:c.3727_3728delinsAC
ENST00000420124.2:c.6405_6406delinsAC	ENSP00000398837.1:p.Ser2135=
NM_014727.2:c.6405_6406delinsAC	NP_055542.1:p.Ser2135=
XM_011527561.1:c.6339_6340delinsAC	XP_011525863.1:p.Ser2113=
XM_011527562.1:c.6405_6406delinsAC	XP_011525864.1:p.Ser2135=
XM_011527563.1:c.6129_6130delinsAC	XP_011525865.1:p.Ser2043=
XM_011527561.2:c.5841_5842delinsAC	XP_011525863.2:p.Ser1947=
XM_011527562.2:c.6405_6406delinsAC	XP_011525864.1:p.Ser2135=
XM_017027544.1:c.6405_6406delinsAC	XP_016883033.1:p.Ser2135=
XM_017027545.1:c.5841_5842delinsAC	XP_016883034.1:p.Ser1947=
XM_017027546.1:c.3369_3370delinsAC	XP_016883035.1:p.Ser1123=
NM_014727.3:c.6405_6406delinsAC MANE Select	NP_055542.1:p.Ser2135=