Canonical Allele Identifier: CA2003527608

Gene: KMT2A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118503224T= , CM000673.2:g.118503224T=	GRCh38
NC_000011.9:g.118373939T= , CM000673.1:g.118373939T=	GRCh37
NC_000011.8:g.117879149T=	NCBI36
NG_027813.1:g.71735T= , LRG_613:g.71735T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000531904.7:c.7431T=	ENSP00000432391.3:p.His2477=
ENST00000710560.1:c.7422T=	ENSP00000518343.1:p.His2474=
ENST00000649878.2:c.1371T=	ENSP00000497891.2:p.His457=
ENST00000685397.1:c.1371T=	ENSP00000509586.1:p.His457=
ENST00000686370.1:c.1371T=	ENSP00000509179.1:p.His457=
ENST00000689424.1:c.1629T=	ENSP00000509852.1:p.His543=
ENST00000691053.1:c.7404T=	ENSP00000509168.1:p.His2468=
ENST00000389506.10:c.7323T=	ENSP00000374157.5:p.His2441=
ENST00000528278.2:n.6674T=
ENST00000534358.8:c.7332T= MANE Select	ENSP00000436786.2:p.His2444=
ENST00000649699.1:c.7209T=	ENSP00000496927.1:p.His2403=
ENST00000389506.9:c.7323T=	ENSP00000374157.5:p.His2441=
ENST00000528278.1:n.1459T=
ENST00000534358.5:c.7332T=	ENSP00000436786.1:p.His2444=
NM_001197104.1:c.7332T= , LRG_613t1:c.7332T=	NP_001184033.1:p.His2444=
NM_005933.3:c.7323T=	NP_005924.2:p.His2441=
XM_006718839.2:c.4815T=	XP_006718902.2:p.His1605=
XM_011542829.1:c.7431T=	XP_011541131.1:p.His2477=
XM_011542830.1:c.7428T=	XP_011541132.1:p.His2476=
XM_011542831.1:c.7422T=	XP_011541133.1:p.His2474=
XM_011542832.1:c.5238T=	XP_011541134.1:p.His1746=
XM_011542833.1:c.4914T=	XP_011541135.1:p.His1638=
XM_006718839.3:c.4815T=	XP_006718902.2:p.His1605=
XM_011542829.2:c.7431T=	XP_011541131.1:p.His2477=
XM_011542830.2:c.7428T=	XP_011541132.1:p.His2476=
XM_011542831.2:c.7422T=	XP_011541133.1:p.His2474=
XM_011542833.2:c.4914T=	XP_011541135.1:p.His1638=
NM_001197104.2:c.7332T= MANE Select	NP_001184033.1:p.His2444=
NM_005933.4:c.7323T=	NP_005924.2:p.His2441=