Canonical Allele Identifier: CA2003527749

Gene: KMT2A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118503340A= , CM000673.2:g.118503340A=	GRCh38
NC_000011.9:g.118374055A= , CM000673.1:g.118374055A=	GRCh37
NC_000011.8:g.117879265A=	NCBI36
NG_027813.1:g.71851A= , LRG_613:g.71851A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000531904.7:c.7547A=	ENSP00000432391.3:p.Asn2516=
ENST00000710560.1:c.7538A=	ENSP00000518343.1:p.Asn2513=
ENST00000649878.2:c.1487A=	ENSP00000497891.2:p.Asn496=
ENST00000685397.1:c.1487A=	ENSP00000509586.1:p.Asn496=
ENST00000686370.1:c.1487A=	ENSP00000509179.1:p.Asn496=
ENST00000689424.1:c.1745A=	ENSP00000509852.1:p.Asn582=
ENST00000691053.1:c.7520A=	ENSP00000509168.1:p.Asn2507=
ENST00000389506.10:c.7439A=	ENSP00000374157.5:p.Asn2480=
ENST00000528278.2:n.6790A=
ENST00000534358.8:c.7448A= MANE Select	ENSP00000436786.2:p.Asn2483=
ENST00000649699.1:c.7325A=	ENSP00000496927.1:p.Asn2442=
ENST00000389506.9:c.7439A=	ENSP00000374157.5:p.Asn2480=
ENST00000528278.1:n.1575A=
ENST00000534358.5:c.7448A=	ENSP00000436786.1:p.Asn2483=
NM_001197104.1:c.7448A= , LRG_613t1:c.7448A=	NP_001184033.1:p.Asn2483=
NM_005933.3:c.7439A=	NP_005924.2:p.Asn2480=
XM_006718839.2:c.4931A=	XP_006718902.2:p.Asn1644=
XM_011542829.1:c.7547A=	XP_011541131.1:p.Asn2516=
XM_011542830.1:c.7544A=	XP_011541132.1:p.Asn2515=
XM_011542831.1:c.7538A=	XP_011541133.1:p.Asn2513=
XM_011542832.1:c.5354A=	XP_011541134.1:p.Asn1785=
XM_011542833.1:c.5030A=	XP_011541135.1:p.Asn1677=
XM_006718839.3:c.4931A=	XP_006718902.2:p.Asn1644=
XM_011542829.2:c.7547A=	XP_011541131.1:p.Asn2516=
XM_011542830.2:c.7544A=	XP_011541132.1:p.Asn2515=
XM_011542831.2:c.7538A=	XP_011541133.1:p.Asn2513=
XM_011542833.2:c.5030A=	XP_011541135.1:p.Asn1677=
NM_001197104.2:c.7448A= MANE Select	NP_001184033.1:p.Asn2483=
NM_005933.4:c.7439A=	NP_005924.2:p.Asn2480=