Canonical Allele Identifier: CA2003519084

Gene: KMT2A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118491200C= , CM000673.2:g.118491200C=	GRCh38
NC_000011.9:g.118361915C= , CM000673.1:g.118361915C=	GRCh37
NC_000011.8:g.117867125C=	NCBI36
NG_027813.1:g.59711C= , LRG_613:g.59711C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000531904.7:c.4800C=	ENSP00000432391.3:p.Asn1600=
ENST00000710560.1:c.4800C=	ENSP00000518343.1:p.Asn1600=
ENST00000685498.1:c.477C=	ENSP00000509293.1:p.Asn159=
ENST00000691053.1:c.4701C=	ENSP00000509168.1:p.Asn1567=
ENST00000389506.10:c.4701C=	ENSP00000374157.5:p.Asn1567=
ENST00000534358.8:c.4701C= MANE Select	ENSP00000436786.2:p.Asn1567=
ENST00000649699.1:c.4587C=	ENSP00000496927.1:p.Asn1529=
ENST00000389506.9:c.4701C=	ENSP00000374157.5:p.Asn1567=
ENST00000392873.3:c.837C=	ENSP00000376612.3:p.Asn279=
ENST00000534358.5:c.4701C=	ENSP00000436786.1:p.Asn1567=
NM_001197104.1:c.4701C= , LRG_613t1:c.4701C=	NP_001184033.1:p.Asn1567=
NM_005933.3:c.4701C=	NP_005924.2:p.Asn1567=
XM_006718839.2:c.2184C=	XP_006718902.2:p.Asn728=
XM_011542829.1:c.4800C=	XP_011541131.1:p.Asn1600=
XM_011542830.1:c.4797C=	XP_011541132.1:p.Asn1599=
XM_011542831.1:c.4800C=	XP_011541133.1:p.Asn1600=
XM_011542832.1:c.2607C=	XP_011541134.1:p.Asn869=
XM_011542833.1:c.2283C=	XP_011541135.1:p.Asn761=
XM_006718839.3:c.2184C=	XP_006718902.2:p.Asn728=
XM_011542829.2:c.4800C=	XP_011541131.1:p.Asn1600=
XM_011542830.2:c.4797C=	XP_011541132.1:p.Asn1599=
XM_011542831.2:c.4800C=	XP_011541133.1:p.Asn1600=
XM_011542833.2:c.2283C=	XP_011541135.1:p.Asn761=
NM_001197104.2:c.4701C= MANE Select	NP_001184033.1:p.Asn1567=
NM_005933.4:c.4701C=	NP_005924.2:p.Asn1567=