Canonical Allele Identifier: CA2576757203

Gene: KMT2B

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35732447_35732449dup , CM000681.2:g.35732447_35732449dup	GRCh38
NC_000019.9:g.36223348_36223350dup , CM000681.1:g.36223348_36223350dup	GRCh37
NC_000019.8:g.40915188_40915190dup	NCBI36
NG_052906.1:g.19429_19431dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592092.2:n.204_206dup
ENST00000673918.2:c.5832_5834dup	ENSP00000501283.1:p.Pro1945_Pro1946insPro
ENST00000674114.2:c.3439_3441dup	ENSP00000501039.2:n.3439_3441dup
ENST00000684977.1:c.1116_1118dup	ENSP00000509384.1:p.Pro373_Pro374insPro
ENST00000689544.1:n.1051_1053dup
ENST00000691421.1:c.1119_1121dup	ENSP00000508674.1:p.Pro374_Pro375insPro
ENST00000691855.1:c.5440_5442dup
ENST00000692961.1:c.5898_5900dup	ENSP00000509289.1:p.Pro1967_Pro1968insPro
ENST00000693677.1:c.704+118_704+120dup	ENSP00000509779.1:n.704+118_704+120dup
ENST00000420124.4:c.5898_5900dup MANE Select	ENSP00000398837.2:p.Pro1967_Pro1968insPro
ENST00000673918.1:c.5832_5834dup	ENSP00000501283.1:p.Pro1945_Pro1946insPro
ENST00000674114.1:c.3220_3222dup
ENST00000420124.2:c.5898_5900dup	ENSP00000398837.1:p.Pro1967_Pro1968insPro
NM_014727.2:c.5898_5900dup	NP_055542.1:p.Pro1967_Pro1968insPro
XM_011527561.1:c.5832_5834dup	XP_011525863.1:p.Pro1945_Pro1946insPro
XM_011527562.1:c.5898_5900dup	XP_011525864.1:p.Pro1967_Pro1968insPro
XM_011527563.1:c.5622_5624dup	XP_011525865.1:p.Pro1875_Pro1876insPro
XM_011527561.2:c.5334_5336dup	XP_011525863.2:p.Pro1779_Pro1780insPro
XM_011527562.2:c.5898_5900dup	XP_011525864.1:p.Pro1967_Pro1968insPro
XM_017027544.1:c.5898_5900dup	XP_016883033.1:p.Pro1967_Pro1968insPro
XM_017027545.1:c.5334_5336dup	XP_016883034.1:p.Pro1779_Pro1780insPro
XM_017027546.1:c.2862_2864dup	XP_016883035.1:p.Pro955_Pro956insPro
NM_014727.3:c.5898_5900dup MANE Select	NP_055542.1:p.Pro1967_Pro1968insPro