Canonical Allele Identifier: CA2003527890

Gene: KMT2A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118503444C= , CM000673.2:g.118503444C=	GRCh38
NC_000011.9:g.118374159C= , CM000673.1:g.118374159C=	GRCh37
NC_000011.8:g.117879369C=	NCBI36
NG_027813.1:g.71955C= , LRG_613:g.71955C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000531904.7:c.7651C=	ENSP00000432391.3:p.Pro2551=
ENST00000710560.1:c.7642C=	ENSP00000518343.1:p.Pro2548=
ENST00000649878.2:c.1591C=	ENSP00000497891.2:p.Pro531=
ENST00000685397.1:c.1591C=	ENSP00000509586.1:p.Pro531=
ENST00000686370.1:c.1591C=	ENSP00000509179.1:p.Pro531=
ENST00000689424.1:c.1849C=	ENSP00000509852.1:p.Pro617=
ENST00000691053.1:c.7624C=	ENSP00000509168.1:p.Pro2542=
ENST00000389506.10:c.7543C=	ENSP00000374157.5:p.Pro2515=
ENST00000528278.2:n.6894C=
ENST00000534358.8:c.7552C= MANE Select	ENSP00000436786.2:p.Pro2518=
ENST00000649699.1:c.7429C=	ENSP00000496927.1:p.Pro2477=
ENST00000389506.9:c.7543C=	ENSP00000374157.5:p.Pro2515=
ENST00000528278.1:n.1679C=
ENST00000534358.5:c.7552C=	ENSP00000436786.1:p.Pro2518=
NM_001197104.1:c.7552C= , LRG_613t1:c.7552C=	NP_001184033.1:p.Pro2518=
NM_005933.3:c.7543C=	NP_005924.2:p.Pro2515=
XM_006718839.2:c.5035C=	XP_006718902.2:p.Pro1679=
XM_011542829.1:c.7651C=	XP_011541131.1:p.Pro2551=
XM_011542830.1:c.7648C=	XP_011541132.1:p.Pro2550=
XM_011542831.1:c.7642C=	XP_011541133.1:p.Pro2548=
XM_011542832.1:c.5458C=	XP_011541134.1:p.Pro1820=
XM_011542833.1:c.5134C=	XP_011541135.1:p.Pro1712=
XM_006718839.3:c.5035C=	XP_006718902.2:p.Pro1679=
XM_011542829.2:c.7651C=	XP_011541131.1:p.Pro2551=
XM_011542830.2:c.7648C=	XP_011541132.1:p.Pro2550=
XM_011542831.2:c.7642C=	XP_011541133.1:p.Pro2548=
XM_011542833.2:c.5134C=	XP_011541135.1:p.Pro1712=
NM_001197104.2:c.7552C= MANE Select	NP_001184033.1:p.Pro2518=
NM_005933.4:c.7543C=	NP_005924.2:p.Pro2515=