Canonical Allele Identifier: CA477359369

Gene: KMT2A

Linked Data

• MyVariant Identifiers: chr11:g.118373981T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118503266T>A , CM000673.2:g.118503266T>A	GRCh38
NC_000011.9:g.118373981T>A , CM000673.1:g.118373981T>A	GRCh37
NC_000011.8:g.117879191T>A	NCBI36
NG_027813.1:g.71777T>A , LRG_613:g.71777T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000531904.7:c.7473T>A	ENSP00000432391.3:p.Gly2491=
ENST00000710560.1:c.7464T>A	ENSP00000518343.1:p.Gly2488=
ENST00000649878.2:c.1413T>A	ENSP00000497891.2:p.Gly471=
ENST00000685397.1:c.1413T>A	ENSP00000509586.1:p.Gly471=
ENST00000686370.1:c.1413T>A	ENSP00000509179.1:p.Gly471=
ENST00000689424.1:c.1671T>A	ENSP00000509852.1:p.Gly557=
ENST00000691053.1:c.7446T>A	ENSP00000509168.1:p.Gly2482=
ENST00000389506.10:c.7365T>A	ENSP00000374157.5:p.Gly2455=
ENST00000528278.2:n.6716T>A
ENST00000534358.8:c.7374T>A MANE Select	ENSP00000436786.2:p.Gly2458=
ENST00000649699.1:c.7251T>A	ENSP00000496927.1:p.Gly2417=
ENST00000389506.9:c.7365T>A	ENSP00000374157.5:p.Gly2455=
ENST00000528278.1:n.1501T>A
ENST00000534358.5:c.7374T>A	ENSP00000436786.1:p.Gly2458=
NM_001197104.1:c.7374T>A , LRG_613t1:c.7374T>A	NP_001184033.1:p.Gly2458=
NM_005933.3:c.7365T>A	NP_005924.2:p.Gly2455=
XM_006718839.2:c.4857T>A	XP_006718902.2:p.Gly1619=
XM_011542829.1:c.7473T>A	XP_011541131.1:p.Gly2491=
XM_011542830.1:c.7470T>A	XP_011541132.1:p.Gly2490=
XM_011542831.1:c.7464T>A	XP_011541133.1:p.Gly2488=
XM_011542832.1:c.5280T>A	XP_011541134.1:p.Gly1760=
XM_011542833.1:c.4956T>A	XP_011541135.1:p.Gly1652=
XM_006718839.3:c.4857T>A	XP_006718902.2:p.Gly1619=
XM_011542829.2:c.7473T>A	XP_011541131.1:p.Gly2491=
XM_011542830.2:c.7470T>A	XP_011541132.1:p.Gly2490=
XM_011542831.2:c.7464T>A	XP_011541133.1:p.Gly2488=
XM_011542833.2:c.4956T>A	XP_011541135.1:p.Gly1652=
NM_001197104.2:c.7374T>A MANE Select	NP_001184033.1:p.Gly2458=
NM_005933.4:c.7365T>A	NP_005924.2:p.Gly2455=