Canonical Allele Identifier: CA2003526297

Gene: KMT2A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118502486C= , CM000673.2:g.118502486C=	GRCh38
NC_000011.9:g.118373201C= , CM000673.1:g.118373201C=	GRCh37
NC_000011.8:g.117878411C=	NCBI36
NG_027813.1:g.70997C= , LRG_613:g.70997C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000531904.7:c.6693C=	ENSP00000432391.3:p.His2231=
ENST00000710560.1:c.6684C=	ENSP00000518343.1:p.His2228=
ENST00000649878.2:c.633C=	ENSP00000497891.2:p.His211=
ENST00000685397.1:c.633C=	ENSP00000509586.1:p.His211=
ENST00000686370.1:c.633C=	ENSP00000509179.1:p.His211=
ENST00000689424.1:c.891C=	ENSP00000509852.1:p.His297=
ENST00000691053.1:c.6666C=	ENSP00000509168.1:p.His2222=
ENST00000389506.10:c.6585C=	ENSP00000374157.5:p.His2195=
ENST00000528278.2:n.5936C=
ENST00000534358.8:c.6594C= MANE Select	ENSP00000436786.2:p.His2198=
ENST00000649699.1:c.6471C=	ENSP00000496927.1:p.His2157=
ENST00000389506.9:c.6585C=	ENSP00000374157.5:p.His2195=
ENST00000528278.1:n.721C=
ENST00000534358.5:c.6594C=	ENSP00000436786.1:p.His2198=
NM_001197104.1:c.6594C= , LRG_613t1:c.6594C=	NP_001184033.1:p.His2198=
NM_005933.3:c.6585C=	NP_005924.2:p.His2195=
XM_006718839.2:c.4077C=	XP_006718902.2:p.His1359=
XM_011542829.1:c.6693C=	XP_011541131.1:p.His2231=
XM_011542830.1:c.6690C=	XP_011541132.1:p.His2230=
XM_011542831.1:c.6684C=	XP_011541133.1:p.His2228=
XM_011542832.1:c.4500C=	XP_011541134.1:p.His1500=
XM_011542833.1:c.4176C=	XP_011541135.1:p.His1392=
XM_006718839.3:c.4077C=	XP_006718902.2:p.His1359=
XM_011542829.2:c.6693C=	XP_011541131.1:p.His2231=
XM_011542830.2:c.6690C=	XP_011541132.1:p.His2230=
XM_011542831.2:c.6684C=	XP_011541133.1:p.His2228=
XM_011542833.2:c.4176C=	XP_011541135.1:p.His1392=
NM_001197104.2:c.6594C= MANE Select	NP_001184033.1:p.His2198=
NM_005933.4:c.6585C=	NP_005924.2:p.His2195=