Canonical Allele Identifier: CA2003527674

Gene: KMT2A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118503281G= , CM000673.2:g.118503281G=	GRCh38
NC_000011.9:g.118373996G= , CM000673.1:g.118373996G=	GRCh37
NC_000011.8:g.117879206G=	NCBI36
NG_027813.1:g.71792G= , LRG_613:g.71792G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000531904.7:c.7488G=	ENSP00000432391.3:p.Leu2496=
ENST00000710560.1:c.7479G=	ENSP00000518343.1:p.Leu2493=
ENST00000649878.2:c.1428G=	ENSP00000497891.2:p.Leu476=
ENST00000685397.1:c.1428G=	ENSP00000509586.1:p.Leu476=
ENST00000686370.1:c.1428G=	ENSP00000509179.1:p.Leu476=
ENST00000689424.1:c.1686G=	ENSP00000509852.1:p.Leu562=
ENST00000691053.1:c.7461G=	ENSP00000509168.1:p.Leu2487=
ENST00000389506.10:c.7380G=	ENSP00000374157.5:p.Leu2460=
ENST00000528278.2:n.6731G=
ENST00000534358.8:c.7389G= MANE Select	ENSP00000436786.2:p.Leu2463=
ENST00000649699.1:c.7266G=	ENSP00000496927.1:p.Leu2422=
ENST00000389506.9:c.7380G=	ENSP00000374157.5:p.Leu2460=
ENST00000528278.1:n.1516G=
ENST00000534358.5:c.7389G=	ENSP00000436786.1:p.Leu2463=
NM_001197104.1:c.7389G= , LRG_613t1:c.7389G=	NP_001184033.1:p.Leu2463=
NM_005933.3:c.7380G=	NP_005924.2:p.Leu2460=
XM_006718839.2:c.4872G=	XP_006718902.2:p.Leu1624=
XM_011542829.1:c.7488G=	XP_011541131.1:p.Leu2496=
XM_011542830.1:c.7485G=	XP_011541132.1:p.Leu2495=
XM_011542831.1:c.7479G=	XP_011541133.1:p.Leu2493=
XM_011542832.1:c.5295G=	XP_011541134.1:p.Leu1765=
XM_011542833.1:c.4971G=	XP_011541135.1:p.Leu1657=
XM_006718839.3:c.4872G=	XP_006718902.2:p.Leu1624=
XM_011542829.2:c.7488G=	XP_011541131.1:p.Leu2496=
XM_011542830.2:c.7485G=	XP_011541132.1:p.Leu2495=
XM_011542831.2:c.7479G=	XP_011541133.1:p.Leu2493=
XM_011542833.2:c.4971G=	XP_011541135.1:p.Leu1657=
NM_001197104.2:c.7389G= MANE Select	NP_001184033.1:p.Leu2463=
NM_005933.4:c.7380G=	NP_005924.2:p.Leu2460=