Canonical Allele Identifier: CA2580096821

Gene: KMT2B

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35718300_35718317dup , CM000681.2:g.35718300_35718317dup	GRCh38
NC_000019.9:g.36209202_36209219dup , CM000681.1:g.36209202_36209219dup	GRCh37
NC_000019.8:g.40901042_40901059dup	NCBI36
NG_052906.1:g.5282_5299dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673918.2:c.282_299dup	ENSP00000501283.1:p.Gly100_Trp101insArgGlyArgGlyArgGly
ENST00000687718.1:c.282_299dup	ENSP00000510535.1:p.Gly100_Trp101insArgGlyArgGlyArgGly
ENST00000692961.1:c.282_299dup	ENSP00000509289.1:p.Gly100_Trp101insArgGlyArgGlyArgGly
ENST00000420124.4:c.282_299dup MANE Select	ENSP00000398837.2:p.Gly100_Trp101insArgGlyArgGlyArgGly
ENST00000673918.1:c.282_299dup	ENSP00000501283.1:p.Gly100_Trp101insArgGlyArgGlyArgGly
ENST00000420124.2:c.282_299dup	ENSP00000398837.1:p.Gly100_Trp101insArgGlyArgGlyArgGly
NM_014727.2:c.282_299dup	NP_055542.1:p.Gly100_Trp101insArgGlyArgGlyArgGly
XM_011527561.1:c.282_299dup	XP_011525863.1:p.Gly100_Trp101insArgGlyArgGlyArgGly
XM_011527562.1:c.282_299dup	XP_011525864.1:p.Gly100_Trp101insArgGlyArgGlyArgGly
XM_011527563.1:c.282_299dup	XP_011525865.1:p.Gly100_Trp101insArgGlyArgGlyArgGly
XR_935878.1:n.306_323dup
XM_011527561.2:c.-217_-200dup	XP_011525863.2:n.-217_-200dup
XM_011527562.2:c.282_299dup	XP_011525864.1:p.Gly100_Trp101insArgGlyArgGlyArgGly
XM_017027544.1:c.282_299dup	XP_016883033.1:p.Gly100_Trp101insArgGlyArgGlyArgGly
XM_017027545.1:c.-210_-193dup	XP_016883034.1:n.-210_-193dup
XR_935878.2:n.483_500dup
NM_014727.3:c.282_299dup MANE Select	NP_055542.1:p.Gly100_Trp101insArgGlyArgGlyArgGly