Canonical Allele Identifier: CA382806378

Gene: KMT2A

Linked Data

• MyVariant Identifiers: chr11:g.118374267G>A (hg19) ; chr11:g.118503552G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118503552G>A , CM000673.2:g.118503552G>A	GRCh38
NC_000011.9:g.118374267G>A , CM000673.1:g.118374267G>A	GRCh37
NC_000011.8:g.117879477G>A	NCBI36
NG_027813.1:g.72063G>A , LRG_613:g.72063G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000531904.7:c.7759G>A	ENSP00000432391.3:p.Glu2587Lys
ENST00000710560.1:c.7750G>A	ENSP00000518343.1:p.Glu2584Lys
ENST00000649878.2:c.1699G>A	ENSP00000497891.2:p.Glu567Lys
ENST00000685397.1:c.1699G>A	ENSP00000509586.1:p.Glu567Lys
ENST00000686370.1:c.1699G>A	ENSP00000509179.1:p.Glu567Lys
ENST00000689424.1:c.1957G>A	ENSP00000509852.1:p.Glu653Lys
ENST00000691053.1:c.7732G>A	ENSP00000509168.1:p.Glu2578Lys
ENST00000389506.10:c.7651G>A	ENSP00000374157.5:p.Glu2551Lys
ENST00000528278.2:n.7002G>A
ENST00000534358.8:c.7660G>A MANE Select	ENSP00000436786.2:p.Glu2554Lys
ENST00000649699.1:c.7537G>A	ENSP00000496927.1:p.Glu2513Lys
ENST00000389506.9:c.7651G>A	ENSP00000374157.5:p.Glu2551Lys
ENST00000528278.1:n.1787G>A
ENST00000534358.5:c.7660G>A	ENSP00000436786.1:p.Glu2554Lys
NM_001197104.1:c.7660G>A , LRG_613t1:c.7660G>A	NP_001184033.1:p.Glu2554Lys
NM_005933.3:c.7651G>A	NP_005924.2:p.Glu2551Lys
XM_006718839.2:c.5143G>A	XP_006718902.2:p.Glu1715Lys
XM_011542829.1:c.7759G>A	XP_011541131.1:p.Glu2587Lys
XM_011542830.1:c.7756G>A	XP_011541132.1:p.Glu2586Lys
XM_011542831.1:c.7750G>A	XP_011541133.1:p.Glu2584Lys
XM_011542832.1:c.5566G>A	XP_011541134.1:p.Glu1856Lys
XM_011542833.1:c.5242G>A	XP_011541135.1:p.Glu1748Lys
XM_006718839.3:c.5143G>A	XP_006718902.2:p.Glu1715Lys
XM_011542829.2:c.7759G>A	XP_011541131.1:p.Glu2587Lys
XM_011542830.2:c.7756G>A	XP_011541132.1:p.Glu2586Lys
XM_011542831.2:c.7750G>A	XP_011541133.1:p.Glu2584Lys
XM_011542833.2:c.5242G>A	XP_011541135.1:p.Glu1748Lys
NM_001197104.2:c.7660G>A MANE Select	NP_001184033.1:p.Glu2554Lys
NM_005933.4:c.7651G>A	NP_005924.2:p.Glu2551Lys