Canonical Allele Identifier: CA2003527454

Gene: KMT2A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118503143C= , CM000673.2:g.118503143C=	GRCh38
NC_000011.9:g.118373858C= , CM000673.1:g.118373858C=	GRCh37
NC_000011.8:g.117879068C=	NCBI36
NG_027813.1:g.71654C= , LRG_613:g.71654C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000531904.7:c.7350C=	ENSP00000432391.3:p.Ile2450=
ENST00000710560.1:c.7341C=	ENSP00000518343.1:p.Ile2447=
ENST00000649878.2:c.1290C=	ENSP00000497891.2:p.Ile430=
ENST00000685397.1:c.1290C=	ENSP00000509586.1:p.Ile430=
ENST00000686370.1:c.1290C=	ENSP00000509179.1:p.Ile430=
ENST00000689424.1:c.1548C=	ENSP00000509852.1:p.Ile516=
ENST00000691053.1:c.7323C=	ENSP00000509168.1:p.Ile2441=
ENST00000389506.10:c.7242C=	ENSP00000374157.5:p.Ile2414=
ENST00000528278.2:n.6593C=
ENST00000534358.8:c.7251C= MANE Select	ENSP00000436786.2:p.Ile2417=
ENST00000649699.1:c.7128C=	ENSP00000496927.1:p.Ile2376=
ENST00000389506.9:c.7242C=	ENSP00000374157.5:p.Ile2414=
ENST00000528278.1:n.1378C=
ENST00000534358.5:c.7251C=	ENSP00000436786.1:p.Ile2417=
NM_001197104.1:c.7251C= , LRG_613t1:c.7251C=	NP_001184033.1:p.Ile2417=
NM_005933.3:c.7242C=	NP_005924.2:p.Ile2414=
XM_006718839.2:c.4734C=	XP_006718902.2:p.Ile1578=
XM_011542829.1:c.7350C=	XP_011541131.1:p.Ile2450=
XM_011542830.1:c.7347C=	XP_011541132.1:p.Ile2449=
XM_011542831.1:c.7341C=	XP_011541133.1:p.Ile2447=
XM_011542832.1:c.5157C=	XP_011541134.1:p.Ile1719=
XM_011542833.1:c.4833C=	XP_011541135.1:p.Ile1611=
XM_006718839.3:c.4734C=	XP_006718902.2:p.Ile1578=
XM_011542829.2:c.7350C=	XP_011541131.1:p.Ile2450=
XM_011542830.2:c.7347C=	XP_011541132.1:p.Ile2449=
XM_011542831.2:c.7341C=	XP_011541133.1:p.Ile2447=
XM_011542833.2:c.4833C=	XP_011541135.1:p.Ile1611=
NM_001197104.2:c.7251C= MANE Select	NP_001184033.1:p.Ile2417=
NM_005933.4:c.7242C=	NP_005924.2:p.Ile2414=