Canonical Allele Identifier: CA2333794458

Gene: KMT2B

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35732702_35732704delinsTAC , CM000681.2:g.35732702_35732704delinsTAC	GRCh38
NC_000019.9:g.36223603_36223605delinsTAC , CM000681.1:g.36223603_36223605delinsTAC	GRCh37
NC_000019.8:g.40915443_40915445delinsTAC	NCBI36
NG_052906.1:g.19684_19686delinsTAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592092.2:n.459_461delinsTAC
ENST00000673918.2:c.6087_6089delinsTAC	ENSP00000501283.1:p.Ala2029=
ENST00000674114.2:c.3694_3696delinsTAC	ENSP00000501039.2:n.3694_3696delinsTAC
ENST00000684977.1:c.1371_1373delinsTAC	ENSP00000509384.1:p.Ala457=
ENST00000689544.1:n.1306_1308delinsTAC
ENST00000691421.1:c.1374_1376delinsTAC	ENSP00000508674.1:p.Ala458=
ENST00000691855.1:c.5695_5697delinsTAC
ENST00000692961.1:c.6153_6155delinsTAC	ENSP00000509289.1:p.Ala2051=
ENST00000693677.1:c.704+373_704+375delinsTAC	ENSP00000509779.1:n.704+373_704+375delinsTAC
ENST00000420124.4:c.6153_6155delinsTAC MANE Select	ENSP00000398837.2:p.Ala2051=
ENST00000673918.1:c.6087_6089delinsTAC	ENSP00000501283.1:p.Ala2029=
ENST00000674114.1:c.3475_3477delinsTAC
ENST00000420124.2:c.6153_6155delinsTAC	ENSP00000398837.1:p.Ala2051=
NM_014727.2:c.6153_6155delinsTAC	NP_055542.1:p.Ala2051=
XM_011527561.1:c.6087_6089delinsTAC	XP_011525863.1:p.Ala2029=
XM_011527562.1:c.6153_6155delinsTAC	XP_011525864.1:p.Ala2051=
XM_011527563.1:c.5877_5879delinsTAC	XP_011525865.1:p.Ala1959=
XM_011527561.2:c.5589_5591delinsTAC	XP_011525863.2:p.Ala1863=
XM_011527562.2:c.6153_6155delinsTAC	XP_011525864.1:p.Ala2051=
XM_017027544.1:c.6153_6155delinsTAC	XP_016883033.1:p.Ala2051=
XM_017027545.1:c.5589_5591delinsTAC	XP_016883034.1:p.Ala1863=
XM_017027546.1:c.3117_3119delinsTAC	XP_016883035.1:p.Ala1039=
NM_014727.3:c.6153_6155delinsTAC MANE Select	NP_055542.1:p.Ala2051=