Canonical Allele Identifier: CA2003527936

Gene: KMT2A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118503474A= , CM000673.2:g.118503474A=	GRCh38
NC_000011.9:g.118374189A= , CM000673.1:g.118374189A=	GRCh37
NC_000011.8:g.117879399A=	NCBI36
NG_027813.1:g.71985A= , LRG_613:g.71985A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000531904.7:c.7681A=	ENSP00000432391.3:p.Thr2561=
ENST00000710560.1:c.7672A=	ENSP00000518343.1:p.Thr2558=
ENST00000649878.2:c.1621A=	ENSP00000497891.2:p.Thr541=
ENST00000685397.1:c.1621A=	ENSP00000509586.1:p.Thr541=
ENST00000686370.1:c.1621A=	ENSP00000509179.1:p.Thr541=
ENST00000689424.1:c.1879A=	ENSP00000509852.1:p.Thr627=
ENST00000691053.1:c.7654A=	ENSP00000509168.1:p.Thr2552=
ENST00000389506.10:c.7573A=	ENSP00000374157.5:p.Thr2525=
ENST00000528278.2:n.6924A=
ENST00000534358.8:c.7582A= MANE Select	ENSP00000436786.2:p.Thr2528=
ENST00000649699.1:c.7459A=	ENSP00000496927.1:p.Thr2487=
ENST00000389506.9:c.7573A=	ENSP00000374157.5:p.Thr2525=
ENST00000528278.1:n.1709A=
ENST00000534358.5:c.7582A=	ENSP00000436786.1:p.Thr2528=
NM_001197104.1:c.7582A= , LRG_613t1:c.7582A=	NP_001184033.1:p.Thr2528=
NM_005933.3:c.7573A=	NP_005924.2:p.Thr2525=
XM_006718839.2:c.5065A=	XP_006718902.2:p.Thr1689=
XM_011542829.1:c.7681A=	XP_011541131.1:p.Thr2561=
XM_011542830.1:c.7678A=	XP_011541132.1:p.Thr2560=
XM_011542831.1:c.7672A=	XP_011541133.1:p.Thr2558=
XM_011542832.1:c.5488A=	XP_011541134.1:p.Thr1830=
XM_011542833.1:c.5164A=	XP_011541135.1:p.Thr1722=
XM_006718839.3:c.5065A=	XP_006718902.2:p.Thr1689=
XM_011542829.2:c.7681A=	XP_011541131.1:p.Thr2561=
XM_011542830.2:c.7678A=	XP_011541132.1:p.Thr2560=
XM_011542831.2:c.7672A=	XP_011541133.1:p.Thr2558=
XM_011542833.2:c.5164A=	XP_011541135.1:p.Thr1722=
NM_001197104.2:c.7582A= MANE Select	NP_001184033.1:p.Thr2528=
NM_005933.4:c.7573A=	NP_005924.2:p.Thr2525=