Canonical Allele Identifier: CA2003526330

Gene: KMT2A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118502505C= , CM000673.2:g.118502505C=	GRCh38
NC_000011.9:g.118373220C= , CM000673.1:g.118373220C=	GRCh37
NC_000011.8:g.117878430C=	NCBI36
NG_027813.1:g.71016C= , LRG_613:g.71016C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000531904.7:c.6712C=	ENSP00000432391.3:p.Pro2238=
ENST00000710560.1:c.6703C=	ENSP00000518343.1:p.Pro2235=
ENST00000649878.2:c.652C=	ENSP00000497891.2:p.Pro218=
ENST00000685397.1:c.652C=	ENSP00000509586.1:p.Pro218=
ENST00000686370.1:c.652C=	ENSP00000509179.1:p.Pro218=
ENST00000689424.1:c.910C=	ENSP00000509852.1:p.Pro304=
ENST00000691053.1:c.6685C=	ENSP00000509168.1:p.Pro2229=
ENST00000389506.10:c.6604C=	ENSP00000374157.5:p.Pro2202=
ENST00000528278.2:n.5955C=
ENST00000534358.8:c.6613C= MANE Select	ENSP00000436786.2:p.Pro2205=
ENST00000649699.1:c.6490C=	ENSP00000496927.1:p.Pro2164=
ENST00000389506.9:c.6604C=	ENSP00000374157.5:p.Pro2202=
ENST00000528278.1:n.740C=
ENST00000534358.5:c.6613C=	ENSP00000436786.1:p.Pro2205=
NM_001197104.1:c.6613C= , LRG_613t1:c.6613C=	NP_001184033.1:p.Pro2205=
NM_005933.3:c.6604C=	NP_005924.2:p.Pro2202=
XM_006718839.2:c.4096C=	XP_006718902.2:p.Pro1366=
XM_011542829.1:c.6712C=	XP_011541131.1:p.Pro2238=
XM_011542830.1:c.6709C=	XP_011541132.1:p.Pro2237=
XM_011542831.1:c.6703C=	XP_011541133.1:p.Pro2235=
XM_011542832.1:c.4519C=	XP_011541134.1:p.Pro1507=
XM_011542833.1:c.4195C=	XP_011541135.1:p.Pro1399=
XM_006718839.3:c.4096C=	XP_006718902.2:p.Pro1366=
XM_011542829.2:c.6712C=	XP_011541131.1:p.Pro2238=
XM_011542830.2:c.6709C=	XP_011541132.1:p.Pro2237=
XM_011542831.2:c.6703C=	XP_011541133.1:p.Pro2235=
XM_011542833.2:c.4195C=	XP_011541135.1:p.Pro1399=
NM_001197104.2:c.6613C= MANE Select	NP_001184033.1:p.Pro2205=
NM_005933.4:c.6604C=	NP_005924.2:p.Pro2202=