Canonical Allele Identifier: CA2003527489

Gene: KMT2A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118503154T= , CM000673.2:g.118503154T=	GRCh38
NC_000011.9:g.118373869T= , CM000673.1:g.118373869T=	GRCh37
NC_000011.8:g.117879079T=	NCBI36
NG_027813.1:g.71665T= , LRG_613:g.71665T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000531904.7:c.7361T=	ENSP00000432391.3:p.Met2454=
ENST00000710560.1:c.7352T=	ENSP00000518343.1:p.Met2451=
ENST00000649878.2:c.1301T=	ENSP00000497891.2:p.Met434=
ENST00000685397.1:c.1301T=	ENSP00000509586.1:p.Met434=
ENST00000686370.1:c.1301T=	ENSP00000509179.1:p.Met434=
ENST00000689424.1:c.1559T=	ENSP00000509852.1:p.Met520=
ENST00000691053.1:c.7334T=	ENSP00000509168.1:p.Met2445=
ENST00000389506.10:c.7253T=	ENSP00000374157.5:p.Met2418=
ENST00000528278.2:n.6604T=
ENST00000534358.8:c.7262T= MANE Select	ENSP00000436786.2:p.Met2421=
ENST00000649699.1:c.7139T=	ENSP00000496927.1:p.Met2380=
ENST00000389506.9:c.7253T=	ENSP00000374157.5:p.Met2418=
ENST00000528278.1:n.1389T=
ENST00000534358.5:c.7262T=	ENSP00000436786.1:p.Met2421=
NM_001197104.1:c.7262T= , LRG_613t1:c.7262T=	NP_001184033.1:p.Met2421=
NM_005933.3:c.7253T=	NP_005924.2:p.Met2418=
XM_006718839.2:c.4745T=	XP_006718902.2:p.Met1582=
XM_011542829.1:c.7361T=	XP_011541131.1:p.Met2454=
XM_011542830.1:c.7358T=	XP_011541132.1:p.Met2453=
XM_011542831.1:c.7352T=	XP_011541133.1:p.Met2451=
XM_011542832.1:c.5168T=	XP_011541134.1:p.Met1723=
XM_011542833.1:c.4844T=	XP_011541135.1:p.Met1615=
XM_006718839.3:c.4745T=	XP_006718902.2:p.Met1582=
XM_011542829.2:c.7361T=	XP_011541131.1:p.Met2454=
XM_011542830.2:c.7358T=	XP_011541132.1:p.Met2453=
XM_011542831.2:c.7352T=	XP_011541133.1:p.Met2451=
XM_011542833.2:c.4844T=	XP_011541135.1:p.Met1615=
NM_001197104.2:c.7262T= MANE Select	NP_001184033.1:p.Met2421=
NM_005933.4:c.7253T=	NP_005924.2:p.Met2418=