Canonical Allele Identifier: CA2003527600

Gene: KMT2A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118503222C= , CM000673.2:g.118503222C=	GRCh38
NC_000011.9:g.118373937C= , CM000673.1:g.118373937C=	GRCh37
NC_000011.8:g.117879147C=	NCBI36
NG_027813.1:g.71733C= , LRG_613:g.71733C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000531904.7:c.7429C=	ENSP00000432391.3:p.His2477=
ENST00000710560.1:c.7420C=	ENSP00000518343.1:p.His2474=
ENST00000649878.2:c.1369C=	ENSP00000497891.2:p.His457=
ENST00000685397.1:c.1369C=	ENSP00000509586.1:p.His457=
ENST00000686370.1:c.1369C=	ENSP00000509179.1:p.His457=
ENST00000689424.1:c.1627C=	ENSP00000509852.1:p.His543=
ENST00000691053.1:c.7402C=	ENSP00000509168.1:p.His2468=
ENST00000389506.10:c.7321C=	ENSP00000374157.5:p.His2441=
ENST00000528278.2:n.6672C=
ENST00000534358.8:c.7330C= MANE Select	ENSP00000436786.2:p.His2444=
ENST00000649699.1:c.7207C=	ENSP00000496927.1:p.His2403=
ENST00000389506.9:c.7321C=	ENSP00000374157.5:p.His2441=
ENST00000528278.1:n.1457C=
ENST00000534358.5:c.7330C=	ENSP00000436786.1:p.His2444=
NM_001197104.1:c.7330C= , LRG_613t1:c.7330C=	NP_001184033.1:p.His2444=
NM_005933.3:c.7321C=	NP_005924.2:p.His2441=
XM_006718839.2:c.4813C=	XP_006718902.2:p.His1605=
XM_011542829.1:c.7429C=	XP_011541131.1:p.His2477=
XM_011542830.1:c.7426C=	XP_011541132.1:p.His2476=
XM_011542831.1:c.7420C=	XP_011541133.1:p.His2474=
XM_011542832.1:c.5236C=	XP_011541134.1:p.His1746=
XM_011542833.1:c.4912C=	XP_011541135.1:p.His1638=
XM_006718839.3:c.4813C=	XP_006718902.2:p.His1605=
XM_011542829.2:c.7429C=	XP_011541131.1:p.His2477=
XM_011542830.2:c.7426C=	XP_011541132.1:p.His2476=
XM_011542831.2:c.7420C=	XP_011541133.1:p.His2474=
XM_011542833.2:c.4912C=	XP_011541135.1:p.His1638=
NM_001197104.2:c.7330C= MANE Select	NP_001184033.1:p.His2444=
NM_005933.4:c.7321C=	NP_005924.2:p.His2441=