Canonical Allele Identifier: CA477092217

Gene: KMT2A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118498525C>T , CM000673.2:g.118498525C>T	GRCh38
NC_000011.9:g.118369240C>T , CM000673.1:g.118369240C>T	GRCh37
NC_000011.8:g.117874450C>T	NCBI36
NG_027813.1:g.67036C>T , LRG_613:g.67036C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001197104.2:c.5958C>T MANE Select	NP_001184033.1:p.Gly1986=
ENST00000534358.8:c.5958C>T MANE Select	ENSP00000436786.2:p.Gly1986=
NM_001197104.1:c.5958C>T , LRG_613t1:c.5958C>T	NP_001184033.1:p.Gly1986=
NM_005933.3:c.5949C>T	NP_005924.2:p.Gly1983=
NM_005933.4:c.5949C>T	NP_005924.2:p.Gly1983=
ENST00000389506.10:c.5949C>T	ENSP00000374157.5:p.Gly1983=
ENST00000389506.9:c.5949C>T	ENSP00000374157.5:p.Gly1983=
ENST00000528278.2:n.3039C>T
ENST00000531904.7:c.6057C>T	ENSP00000432391.3:p.Gly2019=
ENST00000534358.5:c.5958C>T	ENSP00000436786.1:p.Gly1986=
ENST00000649699.1:c.5835C>T	ENSP00000496927.1:p.Gly1945=
ENST00000689424.1:c.258+36C>T	ENSP00000509852.1:n.258+36C>T
ENST00000691053.1:c.6030C>T	ENSP00000509168.1:p.Gly2010=
ENST00000710560.1:c.6048C>T	ENSP00000518343.1:p.Gly2016=
XM_006718839.2:c.3441C>T	XP_006718902.2:p.Gly1147=
XM_006718839.3:c.3441C>T	XP_006718902.2:p.Gly1147=
XM_011542829.1:c.6057C>T	XP_011541131.1:p.Gly2019=
XM_011542829.2:c.6057C>T	XP_011541131.1:p.Gly2019=
XM_011542830.1:c.6054C>T	XP_011541132.1:p.Gly2018=
XM_011542830.2:c.6054C>T	XP_011541132.1:p.Gly2018=
XM_011542831.1:c.6048C>T	XP_011541133.1:p.Gly2016=
XM_011542831.2:c.6048C>T	XP_011541133.1:p.Gly2016=
XM_011542832.1:c.3864C>T	XP_011541134.1:p.Gly1288=
XM_011542833.1:c.3540C>T	XP_011541135.1:p.Gly1180=
XM_011542833.2:c.3540C>T	XP_011541135.1:p.Gly1180=