Canonical Allele Identifier: CA382796809

Gene: KMT2A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118496275C>T , CM000673.2:g.118496275C>T	GRCh38
NC_000011.9:g.118366990C>T , CM000673.1:g.118366990C>T	GRCh37
NC_000011.8:g.117872200C>T	NCBI36
NG_027813.1:g.64786C>T , LRG_613:g.64786C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001197104.2:c.5572C>T MANE Select	NP_001184033.1:p.Arg1858Ter
ENST00000534358.8:c.5572C>T MANE Select	ENSP00000436786.2:p.Arg1858Ter
NM_001197104.1:c.5572C>T , LRG_613t1:c.5572C>T	NP_001184033.1:p.Arg1858Ter
NM_005933.3:c.5563C>T	NP_005924.2:p.Arg1855Ter
NM_005933.4:c.5563C>T	NP_005924.2:p.Arg1855Ter
ENST00000389506.10:c.5563C>T	ENSP00000374157.5:p.Arg1855Ter
ENST00000389506.9:c.5563C>T	ENSP00000374157.5:p.Arg1855Ter
ENST00000528278.2:n.1085C>T
ENST00000531904.7:c.5671C>T	ENSP00000432391.3:p.Arg1891Ter
ENST00000534358.5:c.5572C>T	ENSP00000436786.1:p.Arg1858Ter
ENST00000649699.1:c.5449C>T	ENSP00000496927.1:p.Arg1817Ter
ENST00000691002.1:c.509C>T
ENST00000691053.1:c.5563C>T	ENSP00000509168.1:p.Arg1855Ter
ENST00000693536.1:c.454C>T
ENST00000710560.1:c.5662C>T	ENSP00000518343.1:p.Arg1888Ter
XM_006718839.2:c.3055C>T	XP_006718902.2:p.Arg1019Ter
XM_006718839.3:c.3055C>T	XP_006718902.2:p.Arg1019Ter
XM_011542829.1:c.5671C>T	XP_011541131.1:p.Arg1891Ter
XM_011542829.2:c.5671C>T	XP_011541131.1:p.Arg1891Ter
XM_011542830.1:c.5668C>T	XP_011541132.1:p.Arg1890Ter
XM_011542830.2:c.5668C>T	XP_011541132.1:p.Arg1890Ter
XM_011542831.1:c.5662C>T	XP_011541133.1:p.Arg1888Ter
XM_011542831.2:c.5662C>T	XP_011541133.1:p.Arg1888Ter
XM_011542832.1:c.3478C>T	XP_011541134.1:p.Arg1160Ter
XM_011542833.1:c.3154C>T	XP_011541135.1:p.Arg1052Ter
XM_011542833.2:c.3154C>T	XP_011541135.1:p.Arg1052Ter