Canonical Allele Identifier: CA2333793090

Gene: KMT2B

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35730014_35730017delinsGTCC , CM000681.2:g.35730014_35730017delinsGTCC	GRCh38
NC_000019.9:g.36220915_36220918delinsGTCC , CM000681.1:g.36220915_36220918delinsGTCC	GRCh37
NC_000019.8:g.40912755_40912758delinsGTCC	NCBI36
NG_052906.1:g.16996_16999delinsGTCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673918.2:c.4899_4902delinsGTCC	ENSP00000501283.1:p.Leu1633=
ENST00000674114.2:c.2506_2509delinsGTCC	ENSP00000501039.2:n.2506_2509delinsGTCC
ENST00000684977.1:c.183_186delinsGTCC	ENSP00000509384.1:p.Leu61=
ENST00000685168.1:c.391_394delinsGTCC
ENST00000689544.1:n.118_121delinsGTCC
ENST00000691421.1:c.186_189delinsGTCC	ENSP00000508674.1:p.Leu62=
ENST00000691855.1:c.4507_4510delinsGTCC
ENST00000692961.1:c.4965_4968delinsGTCC	ENSP00000509289.1:p.Leu1655=
ENST00000420124.4:c.4965_4968delinsGTCC MANE Select	ENSP00000398837.2:p.Leu1655=
ENST00000673918.1:c.4899_4902delinsGTCC	ENSP00000501283.1:p.Leu1633=
ENST00000674114.1:c.2287_2290delinsGTCC
ENST00000420124.2:c.4965_4968delinsGTCC	ENSP00000398837.1:p.Leu1655=
NM_014727.2:c.4965_4968delinsGTCC	NP_055542.1:p.Leu1655=
XM_011527561.1:c.4899_4902delinsGTCC	XP_011525863.1:p.Leu1633=
XM_011527562.1:c.4965_4968delinsGTCC	XP_011525864.1:p.Leu1655=
XM_011527563.1:c.4689_4692delinsGTCC	XP_011525865.1:p.Leu1563=
XM_011527561.2:c.4401_4404delinsGTCC	XP_011525863.2:p.Leu1467=
XM_011527562.2:c.4965_4968delinsGTCC	XP_011525864.1:p.Leu1655=
XM_017027544.1:c.4965_4968delinsGTCC	XP_016883033.1:p.Leu1655=
XM_017027545.1:c.4401_4404delinsGTCC	XP_016883034.1:p.Leu1467=
XM_017027546.1:c.1929_1932delinsGTCC	XP_016883035.1:p.Leu643=
NM_014727.3:c.4965_4968delinsGTCC MANE Select	NP_055542.1:p.Leu1655=