Canonical Allele Identifier: CA477359386

Gene: KMT2A

Linked Data

• MyVariant Identifiers: chr11:g.118373999G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118503284G>A , CM000673.2:g.118503284G>A	GRCh38
NC_000011.9:g.118373999G>A , CM000673.1:g.118373999G>A	GRCh37
NC_000011.8:g.117879209G>A	NCBI36
NG_027813.1:g.71795G>A , LRG_613:g.71795G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000531904.7:c.7491G>A	ENSP00000432391.3:p.Lys2497=
ENST00000710560.1:c.7482G>A	ENSP00000518343.1:p.Lys2494=
ENST00000649878.2:c.1431G>A	ENSP00000497891.2:p.Lys477=
ENST00000685397.1:c.1431G>A	ENSP00000509586.1:p.Lys477=
ENST00000686370.1:c.1431G>A	ENSP00000509179.1:p.Lys477=
ENST00000689424.1:c.1689G>A	ENSP00000509852.1:p.Lys563=
ENST00000691053.1:c.7464G>A	ENSP00000509168.1:p.Lys2488=
ENST00000389506.10:c.7383G>A	ENSP00000374157.5:p.Lys2461=
ENST00000528278.2:n.6734G>A
ENST00000534358.8:c.7392G>A MANE Select	ENSP00000436786.2:p.Lys2464=
ENST00000649699.1:c.7269G>A	ENSP00000496927.1:p.Lys2423=
ENST00000389506.9:c.7383G>A	ENSP00000374157.5:p.Lys2461=
ENST00000528278.1:n.1519G>A
ENST00000534358.5:c.7392G>A	ENSP00000436786.1:p.Lys2464=
NM_001197104.1:c.7392G>A , LRG_613t1:c.7392G>A	NP_001184033.1:p.Lys2464=
NM_005933.3:c.7383G>A	NP_005924.2:p.Lys2461=
XM_006718839.2:c.4875G>A	XP_006718902.2:p.Lys1625=
XM_011542829.1:c.7491G>A	XP_011541131.1:p.Lys2497=
XM_011542830.1:c.7488G>A	XP_011541132.1:p.Lys2496=
XM_011542831.1:c.7482G>A	XP_011541133.1:p.Lys2494=
XM_011542832.1:c.5298G>A	XP_011541134.1:p.Lys1766=
XM_011542833.1:c.4974G>A	XP_011541135.1:p.Lys1658=
XM_006718839.3:c.4875G>A	XP_006718902.2:p.Lys1625=
XM_011542829.2:c.7491G>A	XP_011541131.1:p.Lys2497=
XM_011542830.2:c.7488G>A	XP_011541132.1:p.Lys2496=
XM_011542831.2:c.7482G>A	XP_011541133.1:p.Lys2494=
XM_011542833.2:c.4974G>A	XP_011541135.1:p.Lys1658=
NM_001197104.2:c.7392G>A MANE Select	NP_001184033.1:p.Lys2464=
NM_005933.4:c.7383G>A	NP_005924.2:p.Lys2461=