Canonical Allele Identifier: CA2003526214

Gene: KMT2A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118502457G= , CM000673.2:g.118502457G=	GRCh38
NC_000011.9:g.118373172G= , CM000673.1:g.118373172G=	GRCh37
NC_000011.8:g.117878382G=	NCBI36
NG_027813.1:g.70968G= , LRG_613:g.70968G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000531904.7:c.6664G=	ENSP00000432391.3:p.Gly2222=
ENST00000710560.1:c.6655G=	ENSP00000518343.1:p.Gly2219=
ENST00000649878.2:c.604G=	ENSP00000497891.2:p.Gly202=
ENST00000685397.1:c.604G=	ENSP00000509586.1:p.Gly202=
ENST00000686370.1:c.604G=	ENSP00000509179.1:p.Gly202=
ENST00000689424.1:c.862G=	ENSP00000509852.1:p.Gly288=
ENST00000691053.1:c.6637G=	ENSP00000509168.1:p.Gly2213=
ENST00000389506.10:c.6556G=	ENSP00000374157.5:p.Gly2186=
ENST00000528278.2:n.5907G=
ENST00000534358.8:c.6565G= MANE Select	ENSP00000436786.2:p.Gly2189=
ENST00000649699.1:c.6442G=	ENSP00000496927.1:p.Gly2148=
ENST00000389506.9:c.6556G=	ENSP00000374157.5:p.Gly2186=
ENST00000528278.1:n.692G=
ENST00000534358.5:c.6565G=	ENSP00000436786.1:p.Gly2189=
NM_001197104.1:c.6565G= , LRG_613t1:c.6565G=	NP_001184033.1:p.Gly2189=
NM_005933.3:c.6556G=	NP_005924.2:p.Gly2186=
XM_006718839.2:c.4048G=	XP_006718902.2:p.Gly1350=
XM_011542829.1:c.6664G=	XP_011541131.1:p.Gly2222=
XM_011542830.1:c.6661G=	XP_011541132.1:p.Gly2221=
XM_011542831.1:c.6655G=	XP_011541133.1:p.Gly2219=
XM_011542832.1:c.4471G=	XP_011541134.1:p.Gly1491=
XM_011542833.1:c.4147G=	XP_011541135.1:p.Gly1383=
XM_006718839.3:c.4048G=	XP_006718902.2:p.Gly1350=
XM_011542829.2:c.6664G=	XP_011541131.1:p.Gly2222=
XM_011542830.2:c.6661G=	XP_011541132.1:p.Gly2221=
XM_011542831.2:c.6655G=	XP_011541133.1:p.Gly2219=
XM_011542833.2:c.4147G=	XP_011541135.1:p.Gly1383=
NM_001197104.2:c.6565G= MANE Select	NP_001184033.1:p.Gly2189=
NM_005933.4:c.6556G=	NP_005924.2:p.Gly2186=