Canonical Allele Identifier: CA2003512003

Gene: KMT2A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118480199T= , CM000673.2:g.118480199T=	GRCh38
NC_000011.9:g.118350914T= , CM000673.1:g.118350914T=	GRCh37
NC_000011.8:g.117856124T=	NCBI36
NG_027813.1:g.48710T= , LRG_613:g.48710T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000531904.7:c.3694T=	ENSP00000432391.3:p.Trp1232=
ENST00000710560.1:c.3694T=	ENSP00000518343.1:p.Trp1232=
ENST00000527869.7:c.1177T=	ENSP00000432652.3:p.Trp393=
ENST00000533790.3:c.1078T=	ENSP00000436700.3:p.Trp360=
ENST00000649690.2:c.1402T=	ENSP00000497372.2:p.Trp468=
ENST00000685719.1:c.576T=
ENST00000691053.1:c.3595T=	ENSP00000509168.1:p.Trp1199=
ENST00000389506.10:c.3595T=	ENSP00000374157.5:p.Trp1199=
ENST00000533790.2:c.847T=	ENSP00000436700.2:p.Trp283=
ENST00000534358.8:c.3595T= MANE Select	ENSP00000436786.2:p.Trp1199=
ENST00000648261.1:c.2365T=	ENSP00000498126.1:p.Trp789=
ENST00000649699.1:c.3595T=	ENSP00000496927.1:p.Trp1199=
ENST00000389506.9:c.3595T=	ENSP00000374157.5:p.Trp1199=
ENST00000531904.6:c.3694T=	ENSP00000432391.2:p.Trp1232=
ENST00000534358.5:c.3595T=	ENSP00000436786.1:p.Trp1199=
NM_001197104.1:c.3595T= , LRG_613t1:c.3595T=	NP_001184033.1:p.Trp1199=
NM_005933.3:c.3595T=	NP_005924.2:p.Trp1199=
XM_006718839.2:c.1078T=	XP_006718902.2:p.Trp360=
XM_011542829.1:c.3694T=	XP_011541131.1:p.Trp1232=
XM_011542830.1:c.3694T=	XP_011541132.1:p.Trp1232=
XM_011542831.1:c.3694T=	XP_011541133.1:p.Trp1232=
XM_011542832.1:c.1501T=	XP_011541134.1:p.Trp501=
XM_011542833.1:c.1177T=	XP_011541135.1:p.Trp393=
XM_006718839.3:c.1078T=	XP_006718902.2:p.Trp360=
XM_011542829.2:c.3694T=	XP_011541131.1:p.Trp1232=
XM_011542830.2:c.3694T=	XP_011541132.1:p.Trp1232=
XM_011542831.2:c.3694T=	XP_011541133.1:p.Trp1232=
XM_011542833.2:c.1177T=	XP_011541135.1:p.Trp393=
NM_001197104.2:c.3595T= MANE Select	NP_001184033.1:p.Trp1199=
NM_005933.4:c.3595T=	NP_005924.2:p.Trp1199=