Canonical Allele Identifier: CA2003526211

Gene: KMT2A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118502456T= , CM000673.2:g.118502456T=	GRCh38
NC_000011.9:g.118373171T= , CM000673.1:g.118373171T=	GRCh37
NC_000011.8:g.117878381T=	NCBI36
NG_027813.1:g.70967T= , LRG_613:g.70967T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000531904.7:c.6663T=	ENSP00000432391.3:p.Ser2221=
ENST00000710560.1:c.6654T=	ENSP00000518343.1:p.Ser2218=
ENST00000649878.2:c.603T=	ENSP00000497891.2:p.Ser201=
ENST00000685397.1:c.603T=	ENSP00000509586.1:p.Ser201=
ENST00000686370.1:c.603T=	ENSP00000509179.1:p.Ser201=
ENST00000689424.1:c.861T=	ENSP00000509852.1:p.Ser287=
ENST00000691053.1:c.6636T=	ENSP00000509168.1:p.Ser2212=
ENST00000389506.10:c.6555T=	ENSP00000374157.5:p.Ser2185=
ENST00000528278.2:n.5906T=
ENST00000534358.8:c.6564T= MANE Select	ENSP00000436786.2:p.Ser2188=
ENST00000649699.1:c.6441T=	ENSP00000496927.1:p.Ser2147=
ENST00000389506.9:c.6555T=	ENSP00000374157.5:p.Ser2185=
ENST00000528278.1:n.691T=
ENST00000534358.5:c.6564T=	ENSP00000436786.1:p.Ser2188=
NM_001197104.1:c.6564T= , LRG_613t1:c.6564T=	NP_001184033.1:p.Ser2188=
NM_005933.3:c.6555T=	NP_005924.2:p.Ser2185=
XM_006718839.2:c.4047T=	XP_006718902.2:p.Ser1349=
XM_011542829.1:c.6663T=	XP_011541131.1:p.Ser2221=
XM_011542830.1:c.6660T=	XP_011541132.1:p.Ser2220=
XM_011542831.1:c.6654T=	XP_011541133.1:p.Ser2218=
XM_011542832.1:c.4470T=	XP_011541134.1:p.Ser1490=
XM_011542833.1:c.4146T=	XP_011541135.1:p.Ser1382=
XM_006718839.3:c.4047T=	XP_006718902.2:p.Ser1349=
XM_011542829.2:c.6663T=	XP_011541131.1:p.Ser2221=
XM_011542830.2:c.6660T=	XP_011541132.1:p.Ser2220=
XM_011542831.2:c.6654T=	XP_011541133.1:p.Ser2218=
XM_011542833.2:c.4146T=	XP_011541135.1:p.Ser1382=
NM_001197104.2:c.6564T= MANE Select	NP_001184033.1:p.Ser2188=
NM_005933.4:c.6555T=	NP_005924.2:p.Ser2185=