Canonical Allele Identifier: CA382801625

Gene: KMT2A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118501731C>T , CM000673.2:g.118501731C>T	GRCh38
NC_000011.9:g.118372446C>T , CM000673.1:g.118372446C>T	GRCh37
NC_000011.8:g.117877656C>T	NCBI36
NG_027813.1:g.70242C>T , LRG_613:g.70242C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001197104.2:c.6379C>T MANE Select	NP_001184033.1:p.Arg2127Ter
ENST00000534358.8:c.6379C>T MANE Select	ENSP00000436786.2:p.Arg2127Ter
NM_001197104.1:c.6379C>T , LRG_613t1:c.6379C>T	NP_001184033.1:p.Arg2127Ter
NM_005933.3:c.6370C>T	NP_005924.2:p.Arg2124Ter
NM_005933.4:c.6370C>T	NP_005924.2:p.Arg2124Ter
ENST00000389506.10:c.6370C>T	ENSP00000374157.5:p.Arg2124Ter
ENST00000389506.9:c.6370C>T	ENSP00000374157.5:p.Arg2124Ter
ENST00000528278.1:n.506C>T
ENST00000528278.2:n.5721C>T
ENST00000531904.7:c.6478C>T	ENSP00000432391.3:p.Arg2160Ter
ENST00000534358.5:c.6379C>T	ENSP00000436786.1:p.Arg2127Ter
ENST00000649699.1:c.6256C>T	ENSP00000496927.1:p.Arg2086Ter
ENST00000649878.2:c.418C>T	ENSP00000497891.2:p.Arg140Ter
ENST00000685397.1:c.418C>T	ENSP00000509586.1:p.Arg140Ter
ENST00000686370.1:c.418C>T	ENSP00000509179.1:p.Arg140Ter
ENST00000689424.1:c.676C>T	ENSP00000509852.1:p.Arg226Ter
ENST00000691053.1:c.6451C>T	ENSP00000509168.1:p.Arg2151Ter
ENST00000710560.1:c.6469C>T	ENSP00000518343.1:p.Arg2157Ter
XM_006718839.2:c.3862C>T	XP_006718902.2:p.Arg1288Ter
XM_006718839.3:c.3862C>T	XP_006718902.2:p.Arg1288Ter
XM_011542829.1:c.6478C>T	XP_011541131.1:p.Arg2160Ter
XM_011542829.2:c.6478C>T	XP_011541131.1:p.Arg2160Ter
XM_011542830.1:c.6475C>T	XP_011541132.1:p.Arg2159Ter
XM_011542830.2:c.6475C>T	XP_011541132.1:p.Arg2159Ter
XM_011542831.1:c.6469C>T	XP_011541133.1:p.Arg2157Ter
XM_011542831.2:c.6469C>T	XP_011541133.1:p.Arg2157Ter
XM_011542832.1:c.4285C>T	XP_011541134.1:p.Arg1429Ter
XM_011542833.1:c.3961C>T	XP_011541135.1:p.Arg1321Ter
XM_011542833.2:c.3961C>T	XP_011541135.1:p.Arg1321Ter