Canonical Allele Identifier: CA2003527472

Gene: KMT2A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118503146C= , CM000673.2:g.118503146C=	GRCh38
NC_000011.9:g.118373861C= , CM000673.1:g.118373861C=	GRCh37
NC_000011.8:g.117879071C=	NCBI36
NG_027813.1:g.71657C= , LRG_613:g.71657C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000531904.7:c.7353C=	ENSP00000432391.3:p.Asn2451=
ENST00000710560.1:c.7344C=	ENSP00000518343.1:p.Asn2448=
ENST00000649878.2:c.1293C=	ENSP00000497891.2:p.Asn431=
ENST00000685397.1:c.1293C=	ENSP00000509586.1:p.Asn431=
ENST00000686370.1:c.1293C=	ENSP00000509179.1:p.Asn431=
ENST00000689424.1:c.1551C=	ENSP00000509852.1:p.Asn517=
ENST00000691053.1:c.7326C=	ENSP00000509168.1:p.Asn2442=
ENST00000389506.10:c.7245C=	ENSP00000374157.5:p.Asn2415=
ENST00000528278.2:n.6596C=
ENST00000534358.8:c.7254C= MANE Select	ENSP00000436786.2:p.Asn2418=
ENST00000649699.1:c.7131C=	ENSP00000496927.1:p.Asn2377=
ENST00000389506.9:c.7245C=	ENSP00000374157.5:p.Asn2415=
ENST00000528278.1:n.1381C=
ENST00000534358.5:c.7254C=	ENSP00000436786.1:p.Asn2418=
NM_001197104.1:c.7254C= , LRG_613t1:c.7254C=	NP_001184033.1:p.Asn2418=
NM_005933.3:c.7245C=	NP_005924.2:p.Asn2415=
XM_006718839.2:c.4737C=	XP_006718902.2:p.Asn1579=
XM_011542829.1:c.7353C=	XP_011541131.1:p.Asn2451=
XM_011542830.1:c.7350C=	XP_011541132.1:p.Asn2450=
XM_011542831.1:c.7344C=	XP_011541133.1:p.Asn2448=
XM_011542832.1:c.5160C=	XP_011541134.1:p.Asn1720=
XM_011542833.1:c.4836C=	XP_011541135.1:p.Asn1612=
XM_006718839.3:c.4737C=	XP_006718902.2:p.Asn1579=
XM_011542829.2:c.7353C=	XP_011541131.1:p.Asn2451=
XM_011542830.2:c.7350C=	XP_011541132.1:p.Asn2450=
XM_011542831.2:c.7344C=	XP_011541133.1:p.Asn2448=
XM_011542833.2:c.4836C=	XP_011541135.1:p.Asn1612=
NM_001197104.2:c.7254C= MANE Select	NP_001184033.1:p.Asn2418=
NM_005933.4:c.7245C=	NP_005924.2:p.Asn2415=