Canonical Allele Identifier: CA2003527502

Gene: KMT2A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118503165T= , CM000673.2:g.118503165T=	GRCh38
NC_000011.9:g.118373880T= , CM000673.1:g.118373880T=	GRCh37
NC_000011.8:g.117879090T=	NCBI36
NG_027813.1:g.71676T= , LRG_613:g.71676T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000531904.7:c.7372T=	ENSP00000432391.3:p.Ser2458=
ENST00000710560.1:c.7363T=	ENSP00000518343.1:p.Ser2455=
ENST00000649878.2:c.1312T=	ENSP00000497891.2:p.Ser438=
ENST00000685397.1:c.1312T=	ENSP00000509586.1:p.Ser438=
ENST00000686370.1:c.1312T=	ENSP00000509179.1:p.Ser438=
ENST00000689424.1:c.1570T=	ENSP00000509852.1:p.Ser524=
ENST00000691053.1:c.7345T=	ENSP00000509168.1:p.Ser2449=
ENST00000389506.10:c.7264T=	ENSP00000374157.5:p.Ser2422=
ENST00000528278.2:n.6615T=
ENST00000534358.8:c.7273T= MANE Select	ENSP00000436786.2:p.Ser2425=
ENST00000649699.1:c.7150T=	ENSP00000496927.1:p.Ser2384=
ENST00000389506.9:c.7264T=	ENSP00000374157.5:p.Ser2422=
ENST00000528278.1:n.1400T=
ENST00000534358.5:c.7273T=	ENSP00000436786.1:p.Ser2425=
NM_001197104.1:c.7273T= , LRG_613t1:c.7273T=	NP_001184033.1:p.Ser2425=
NM_005933.3:c.7264T=	NP_005924.2:p.Ser2422=
XM_006718839.2:c.4756T=	XP_006718902.2:p.Ser1586=
XM_011542829.1:c.7372T=	XP_011541131.1:p.Ser2458=
XM_011542830.1:c.7369T=	XP_011541132.1:p.Ser2457=
XM_011542831.1:c.7363T=	XP_011541133.1:p.Ser2455=
XM_011542832.1:c.5179T=	XP_011541134.1:p.Ser1727=
XM_011542833.1:c.4855T=	XP_011541135.1:p.Ser1619=
XM_006718839.3:c.4756T=	XP_006718902.2:p.Ser1586=
XM_011542829.2:c.7372T=	XP_011541131.1:p.Ser2458=
XM_011542830.2:c.7369T=	XP_011541132.1:p.Ser2457=
XM_011542831.2:c.7363T=	XP_011541133.1:p.Ser2455=
XM_011542833.2:c.4855T=	XP_011541135.1:p.Ser1619=
NM_001197104.2:c.7273T= MANE Select	NP_001184033.1:p.Ser2425=
NM_005933.4:c.7264T=	NP_005924.2:p.Ser2422=