Canonical Allele Identifier: CA2003527713

Gene: KMT2A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118503322T= , CM000673.2:g.118503322T=	GRCh38
NC_000011.9:g.118374037T= , CM000673.1:g.118374037T=	GRCh37
NC_000011.8:g.117879247T=	NCBI36
NG_027813.1:g.71833T= , LRG_613:g.71833T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000531904.7:c.7529T=	ENSP00000432391.3:p.Met2510=
ENST00000710560.1:c.7520T=	ENSP00000518343.1:p.Met2507=
ENST00000649878.2:c.1469T=	ENSP00000497891.2:p.Met490=
ENST00000685397.1:c.1469T=	ENSP00000509586.1:p.Met490=
ENST00000686370.1:c.1469T=	ENSP00000509179.1:p.Met490=
ENST00000689424.1:c.1727T=	ENSP00000509852.1:p.Met576=
ENST00000691053.1:c.7502T=	ENSP00000509168.1:p.Met2501=
ENST00000389506.10:c.7421T=	ENSP00000374157.5:p.Met2474=
ENST00000528278.2:n.6772T=
ENST00000534358.8:c.7430T= MANE Select	ENSP00000436786.2:p.Met2477=
ENST00000649699.1:c.7307T=	ENSP00000496927.1:p.Met2436=
ENST00000389506.9:c.7421T=	ENSP00000374157.5:p.Met2474=
ENST00000528278.1:n.1557T=
ENST00000534358.5:c.7430T=	ENSP00000436786.1:p.Met2477=
NM_001197104.1:c.7430T= , LRG_613t1:c.7430T=	NP_001184033.1:p.Met2477=
NM_005933.3:c.7421T=	NP_005924.2:p.Met2474=
XM_006718839.2:c.4913T=	XP_006718902.2:p.Met1638=
XM_011542829.1:c.7529T=	XP_011541131.1:p.Met2510=
XM_011542830.1:c.7526T=	XP_011541132.1:p.Met2509=
XM_011542831.1:c.7520T=	XP_011541133.1:p.Met2507=
XM_011542832.1:c.5336T=	XP_011541134.1:p.Met1779=
XM_011542833.1:c.5012T=	XP_011541135.1:p.Met1671=
XM_006718839.3:c.4913T=	XP_006718902.2:p.Met1638=
XM_011542829.2:c.7529T=	XP_011541131.1:p.Met2510=
XM_011542830.2:c.7526T=	XP_011541132.1:p.Met2509=
XM_011542831.2:c.7520T=	XP_011541133.1:p.Met2507=
XM_011542833.2:c.5012T=	XP_011541135.1:p.Met1671=
NM_001197104.2:c.7430T= MANE Select	NP_001184033.1:p.Met2477=
NM_005933.4:c.7421T=	NP_005924.2:p.Met2474=