Canonical Allele Identifier: CA2695228598

Gene: KMT2B

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35732431dup , CM000681.2:g.35732431dup	GRCh38
NC_000019.9:g.36223332dup , CM000681.1:g.36223332dup	GRCh37
NC_000019.8:g.40915172dup	NCBI36
NG_052906.1:g.19413dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592092.2:n.188dup
ENST00000673918.2:c.5816dup	ENSP00000501283.1:p.Gly1940TrpfsTer10
ENST00000674114.2:c.3423dup	ENSP00000501039.2:n.3423dup
ENST00000684977.1:c.1100dup	ENSP00000509384.1:p.Gly368TrpfsTer10
ENST00000689544.1:n.1035dup
ENST00000691421.1:c.1103dup	ENSP00000508674.1:p.Gly369TrpfsTer10
ENST00000691855.1:c.5424dup
ENST00000692961.1:c.5882dup	ENSP00000509289.1:p.Gly1962TrpfsTer10
ENST00000693677.1:c.704+102dup	ENSP00000509779.1:n.704+102dup
ENST00000420124.4:c.5882dup MANE Select	ENSP00000398837.2:p.Gly1962TrpfsTer10
ENST00000673918.1:c.5816dup	ENSP00000501283.1:p.Gly1940TrpfsTer10
ENST00000674114.1:c.3204dup
ENST00000420124.2:c.5882dup	ENSP00000398837.1:p.Gly1962TrpfsTer10
NM_014727.2:c.5882dup	NP_055542.1:p.Gly1962TrpfsTer10
XM_011527561.1:c.5816dup	XP_011525863.1:p.Gly1940TrpfsTer10
XM_011527562.1:c.5882dup	XP_011525864.1:p.Gly1962TrpfsTer10
XM_011527563.1:c.5606dup	XP_011525865.1:p.Gly1870TrpfsTer10
XM_011527561.2:c.5318dup	XP_011525863.2:p.Gly1774TrpfsTer10
XM_011527562.2:c.5882dup	XP_011525864.1:p.Gly1962TrpfsTer10
XM_017027544.1:c.5882dup	XP_016883033.1:p.Gly1962TrpfsTer10
XM_017027545.1:c.5318dup	XP_016883034.1:p.Gly1774TrpfsTer10
XM_017027546.1:c.2846dup	XP_016883035.1:p.Gly950TrpfsTer10
NM_014727.3:c.5882dup MANE Select	NP_055542.1:p.Gly1962TrpfsTer10