Canonical Allele Identifier: CA2333794324

Gene: KMT2B

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35732445_35732448delinsTCTC , CM000681.2:g.35732445_35732448delinsTCTC	GRCh38
NC_000019.9:g.36223346_36223349delinsTCTC , CM000681.1:g.36223346_36223349delinsTCTC	GRCh37
NC_000019.8:g.40915186_40915189delinsTCTC	NCBI36
NG_052906.1:g.19427_19430delinsTCTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592092.2:n.202_205delinsTCTC
ENST00000673918.2:c.5830_5833delinsTCTC	ENSP00000501283.1:p.Ser1944=
ENST00000674114.2:c.3437_3440delinsTCTC	ENSP00000501039.2:n.3437_3440delinsTCTC
ENST00000684977.1:c.1114_1117delinsTCTC	ENSP00000509384.1:p.Ser372=
ENST00000689544.1:n.1049_1052delinsTCTC
ENST00000691421.1:c.1117_1120delinsTCTC	ENSP00000508674.1:p.Ser373=
ENST00000691855.1:c.5438_5441delinsTCTC
ENST00000692961.1:c.5896_5899delinsTCTC	ENSP00000509289.1:p.Ser1966=
ENST00000693677.1:c.704+116_704+119delinsTCTC	ENSP00000509779.1:n.704+116_704+119delinsTCTC
ENST00000420124.4:c.5896_5899delinsTCTC MANE Select	ENSP00000398837.2:p.Ser1966=
ENST00000673918.1:c.5830_5833delinsTCTC	ENSP00000501283.1:p.Ser1944=
ENST00000674114.1:c.3218_3221delinsTCTC
ENST00000420124.2:c.5896_5899delinsTCTC	ENSP00000398837.1:p.Ser1966=
NM_014727.2:c.5896_5899delinsTCTC	NP_055542.1:p.Ser1966=
XM_011527561.1:c.5830_5833delinsTCTC	XP_011525863.1:p.Ser1944=
XM_011527562.1:c.5896_5899delinsTCTC	XP_011525864.1:p.Ser1966=
XM_011527563.1:c.5620_5623delinsTCTC	XP_011525865.1:p.Ser1874=
XM_011527561.2:c.5332_5335delinsTCTC	XP_011525863.2:p.Ser1778=
XM_011527562.2:c.5896_5899delinsTCTC	XP_011525864.1:p.Ser1966=
XM_017027544.1:c.5896_5899delinsTCTC	XP_016883033.1:p.Ser1966=
XM_017027545.1:c.5332_5335delinsTCTC	XP_016883034.1:p.Ser1778=
XM_017027546.1:c.2860_2863delinsTCTC	XP_016883035.1:p.Ser954=
NM_014727.3:c.5896_5899delinsTCTC MANE Select	NP_055542.1:p.Ser1966=