Canonical Allele Identifier: CA2003502138

Gene: KMT2A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118436563G= , CM000673.2:g.118436563G=	GRCh38
NC_000011.9:g.118307278G= , CM000673.1:g.118307278G=	GRCh37
NC_000011.8:g.117812488G=	NCBI36
NG_027813.1:g.5074G= , LRG_613:g.5074G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000531904.7:c.51G=	ENSP00000432391.3:p.Gly17=
ENST00000710560.1:c.51G=	ENSP00000518343.1:p.Gly17=
ENST00000527869.7:c.51G=	ENSP00000432652.3:p.Gly17=
ENST00000529852.3:c.51G=	ENSP00000436564.2:p.Gly17=
ENST00000532204.6:c.51G=	ENSP00000434618.2:p.Gly17=
ENST00000533790.3:c.51G=	ENSP00000436700.3:p.Gly17=
ENST00000649666.2:c.51G=	ENSP00000497918.2:p.Gly17=
ENST00000649690.2:c.51G=	ENSP00000497372.2:p.Gly17=
ENST00000691053.1:c.51G=	ENSP00000509168.1:p.Gly17=
ENST00000389506.10:c.51G=	ENSP00000374157.5:p.Gly17=
ENST00000534358.8:c.51G= MANE Select	ENSP00000436786.2:p.Gly17=
ENST00000648261.1:c.-798-32212G=	ENSP00000498126.1:n.-798-32212G=
ENST00000649464.1:c.214-11062G=	ENSP00000497966.1:n.214-11062G=
ENST00000649699.1:c.51G=	ENSP00000496927.1:p.Gly17=
ENST00000389506.9:c.51G=	ENSP00000374157.5:p.Gly17=
ENST00000531904.6:c.51G=	ENSP00000432391.2:p.Gly17=
ENST00000534358.5:c.51G=	ENSP00000436786.1:p.Gly17=
NM_001197104.1:c.51G= , LRG_613t1:c.51G=	NP_001184033.1:p.Gly17=
NM_005933.3:c.51G=	NP_005924.2:p.Gly17=
XM_006718839.2:c.51G=	XP_006718902.2:p.Gly17=
XM_011542829.1:c.51G=	XP_011541131.1:p.Gly17=
XM_011542830.1:c.51G=	XP_011541132.1:p.Gly17=
XM_011542831.1:c.51G=	XP_011541133.1:p.Gly17=
XM_011542832.1:c.51G=	XP_011541134.1:p.Gly17=
XM_011542833.1:c.51G=	XP_011541135.1:p.Gly17=
XM_006718839.3:c.51G=	XP_006718902.2:p.Gly17=
XM_011542829.2:c.51G=	XP_011541131.1:p.Gly17=
XM_011542830.2:c.51G=	XP_011541132.1:p.Gly17=
XM_011542831.2:c.51G=	XP_011541133.1:p.Gly17=
XM_011542833.2:c.51G=	XP_011541135.1:p.Gly17=
NM_001197104.2:c.51G= MANE Select	NP_001184033.1:p.Gly17=
NM_005933.4:c.51G=	NP_005924.2:p.Gly17=