Canonical Allele Identifier: CA2003528006

Gene: KMT2A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118503558A= , CM000673.2:g.118503558A=	GRCh38
NC_000011.9:g.118374273A= , CM000673.1:g.118374273A=	GRCh37
NC_000011.8:g.117879483A=	NCBI36
NG_027813.1:g.72069A= , LRG_613:g.72069A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000531904.7:c.7765A=	ENSP00000432391.3:p.Thr2589=
ENST00000710560.1:c.7756A=	ENSP00000518343.1:p.Thr2586=
ENST00000649878.2:c.1705A=	ENSP00000497891.2:p.Thr569=
ENST00000685397.1:c.1705A=	ENSP00000509586.1:p.Thr569=
ENST00000686370.1:c.1705A=	ENSP00000509179.1:p.Thr569=
ENST00000689424.1:c.1963A=	ENSP00000509852.1:p.Thr655=
ENST00000691053.1:c.7738A=	ENSP00000509168.1:p.Thr2580=
ENST00000389506.10:c.7657A=	ENSP00000374157.5:p.Thr2553=
ENST00000528278.2:n.7008A=
ENST00000534358.8:c.7666A= MANE Select	ENSP00000436786.2:p.Thr2556=
ENST00000649699.1:c.7543A=	ENSP00000496927.1:p.Thr2515=
ENST00000389506.9:c.7657A=	ENSP00000374157.5:p.Thr2553=
ENST00000528278.1:n.1793A=
ENST00000534358.5:c.7666A=	ENSP00000436786.1:p.Thr2556=
NM_001197104.1:c.7666A= , LRG_613t1:c.7666A=	NP_001184033.1:p.Thr2556=
NM_005933.3:c.7657A=	NP_005924.2:p.Thr2553=
XM_006718839.2:c.5149A=	XP_006718902.2:p.Thr1717=
XM_011542829.1:c.7765A=	XP_011541131.1:p.Thr2589=
XM_011542830.1:c.7762A=	XP_011541132.1:p.Thr2588=
XM_011542831.1:c.7756A=	XP_011541133.1:p.Thr2586=
XM_011542832.1:c.5572A=	XP_011541134.1:p.Thr1858=
XM_011542833.1:c.5248A=	XP_011541135.1:p.Thr1750=
XM_006718839.3:c.5149A=	XP_006718902.2:p.Thr1717=
XM_011542829.2:c.7765A=	XP_011541131.1:p.Thr2589=
XM_011542830.2:c.7762A=	XP_011541132.1:p.Thr2588=
XM_011542831.2:c.7756A=	XP_011541133.1:p.Thr2586=
XM_011542833.2:c.5248A=	XP_011541135.1:p.Thr1750=
NM_001197104.2:c.7666A= MANE Select	NP_001184033.1:p.Thr2556=
NM_005933.4:c.7657A=	NP_005924.2:p.Thr2553=