Canonical Allele Identifier: CA2333793016

Gene: KMT2B

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35729849_35729850delinsCT , CM000681.2:g.35729849_35729850delinsCT	GRCh38
NC_000019.9:g.36220750_36220751delinsCT , CM000681.1:g.36220750_36220751delinsCT	GRCh37
NC_000019.8:g.40912590_40912591delinsCT	NCBI36
NG_052906.1:g.16831_16832delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673918.2:c.4852-118_4852-117delinsCT	ENSP00000501283.1:n.4852-118_4852-117delinsCT
ENST00000674114.2:c.2459-118_2459-117delinsCT	ENSP00000501039.2:n.2459-118_2459-117delinsCT
ENST00000684977.1:c.136-118_136-117delinsCT	ENSP00000509384.1:n.136-118_136-117delinsCT
ENST00000685168.1:c.344-118_344-117delinsCT
ENST00000689544.1:n.71-118_71-117delinsCT
ENST00000691421.1:c.139-118_139-117delinsCT	ENSP00000508674.1:n.139-118_139-117delinsCT
ENST00000691855.1:c.4460-118_4460-117delinsCT
ENST00000692961.1:c.4918-118_4918-117delinsCT	ENSP00000509289.1:n.4918-118_4918-117delinsCT
ENST00000420124.4:c.4918-118_4918-117delinsCT MANE Select	ENSP00000398837.2:n.4918-118_4918-117delinsCT
ENST00000673918.1:c.4852-118_4852-117delinsCT	ENSP00000501283.1:n.4852-118_4852-117delinsCT
ENST00000674114.1:c.2240-118_2240-117delinsCT
ENST00000420124.2:c.4918-118_4918-117delinsCT	ENSP00000398837.1:n.4918-118_4918-117delinsCT
NM_014727.2:c.4918-118_4918-117delinsCT	NP_055542.1:n.4918-118_4918-117delinsCT
XM_011527561.1:c.4852-118_4852-117delinsCT	XP_011525863.1:n.4852-118_4852-117delinsCT
XM_011527562.1:c.4918-118_4918-117delinsCT	XP_011525864.1:n.4918-118_4918-117delinsCT
XM_011527563.1:c.4642-118_4642-117delinsCT	XP_011525865.1:n.4642-118_4642-117delinsCT
XM_011527561.2:c.4354-118_4354-117delinsCT	XP_011525863.2:n.4354-118_4354-117delinsCT
XM_011527562.2:c.4918-118_4918-117delinsCT	XP_011525864.1:n.4918-118_4918-117delinsCT
XM_017027544.1:c.4918-118_4918-117delinsCT	XP_016883033.1:n.4918-118_4918-117delinsCT
XM_017027545.1:c.4354-118_4354-117delinsCT	XP_016883034.1:n.4354-118_4354-117delinsCT
XM_017027546.1:c.1882-118_1882-117delinsCT	XP_016883035.1:n.1882-118_1882-117delinsCT
NM_014727.3:c.4918-118_4918-117delinsCT MANE Select	NP_055542.1:n.4918-118_4918-117delinsCT