Canonical Allele Identifier: CA477089578

Gene: KMT2A

Linked Data

• MyVariant Identifiers: chr11:g.118359430T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118488715T>G , CM000673.2:g.118488715T>G	GRCh38
NC_000011.9:g.118359430T>G , CM000673.1:g.118359430T>G	GRCh37
NC_000011.8:g.117864640T>G	NCBI36
NG_027813.1:g.57226T>G , LRG_613:g.57226T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000531904.7:c.4533T>G	ENSP00000432391.3:p.Arg1511=
ENST00000710560.1:c.4533T>G	ENSP00000518343.1:p.Arg1511=
ENST00000420751.4:c.345T>G	ENSP00000510776.1:p.Arg115=
ENST00000685498.1:c.213T>G	ENSP00000509293.1:p.Arg71=
ENST00000691053.1:c.4434T>G	ENSP00000509168.1:p.Arg1478=
ENST00000389506.10:c.4434T>G	ENSP00000374157.5:p.Arg1478=
ENST00000534358.8:c.4434T>G MANE Select	ENSP00000436786.2:p.Arg1478=
ENST00000649699.1:c.4320T>G	ENSP00000496927.1:p.Arg1440=
ENST00000389506.9:c.4434T>G	ENSP00000374157.5:p.Arg1478=
ENST00000392873.3:c.570T>G	ENSP00000376612.3:p.Arg190=
ENST00000534358.5:c.4434T>G	ENSP00000436786.1:p.Arg1478=
NM_001197104.1:c.4434T>G , LRG_613t1:c.4434T>G	NP_001184033.1:p.Arg1478=
NM_005933.3:c.4434T>G	NP_005924.2:p.Arg1478=
XM_006718839.2:c.1917T>G	XP_006718902.2:p.Arg639=
XM_011542829.1:c.4533T>G	XP_011541131.1:p.Arg1511=
XM_011542830.1:c.4533T>G	XP_011541132.1:p.Arg1511=
XM_011542831.1:c.4533T>G	XP_011541133.1:p.Arg1511=
XM_011542832.1:c.2340T>G	XP_011541134.1:p.Arg780=
XM_011542833.1:c.2016T>G	XP_011541135.1:p.Arg672=
XM_006718839.3:c.1917T>G	XP_006718902.2:p.Arg639=
XM_011542829.2:c.4533T>G	XP_011541131.1:p.Arg1511=
XM_011542830.2:c.4533T>G	XP_011541132.1:p.Arg1511=
XM_011542831.2:c.4533T>G	XP_011541133.1:p.Arg1511=
XM_011542833.2:c.2016T>G	XP_011541135.1:p.Arg672=
NM_001197104.2:c.4434T>G MANE Select	NP_001184033.1:p.Arg1478=
NM_005933.4:c.4434T>G	NP_005924.2:p.Arg1478=