Canonical Allele Identifier: CA2003518530

Gene: KMT2A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118490262G= , CM000673.2:g.118490262G=	GRCh38
NC_000011.9:g.118360977G= , CM000673.1:g.118360977G=	GRCh37
NC_000011.8:g.117866187G=	NCBI36
NG_027813.1:g.58773G= , LRG_613:g.58773G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000531904.7:c.4795+13G=	ENSP00000432391.3:n.4795+13G=
ENST00000710560.1:c.4795+13G=	ENSP00000518343.1:n.4795+13G=
ENST00000685498.1:c.472+13G=	ENSP00000509293.1:n.472+13G=
ENST00000691053.1:c.4696+13G=	ENSP00000509168.1:n.4696+13G=
ENST00000389506.10:c.4696+13G=	ENSP00000374157.5:n.4696+13G=
ENST00000534358.8:c.4696+13G= MANE Select	ENSP00000436786.2:n.4696+13G=
ENST00000649699.1:c.4582+13G=	ENSP00000496927.1:n.4582+13G=
ENST00000389506.9:c.4696+13G=	ENSP00000374157.5:n.4696+13G=
ENST00000392873.3:c.832+13G=	ENSP00000376612.3:n.832+13G=
ENST00000534358.5:c.4696+13G=	ENSP00000436786.1:n.4696+13G=
NM_001197104.1:c.4696+13G= , LRG_613t1:c.4696+13G=	NP_001184033.1:n.4696+13G=
NM_005933.3:c.4696+13G=	NP_005924.2:n.4696+13G=
XM_006718839.2:c.2179+13G=	XP_006718902.2:n.2179+13G=
XM_011542829.1:c.4795+13G=	XP_011541131.1:n.4795+13G=
XM_011542830.1:c.4792+13G=	XP_011541132.1:n.4792+13G=
XM_011542831.1:c.4795+13G=	XP_011541133.1:n.4795+13G=
XM_011542832.1:c.2602+13G=	XP_011541134.1:n.2602+13G=
XM_011542833.1:c.2278+13G=	XP_011541135.1:n.2278+13G=
XM_006718839.3:c.2179+13G=	XP_006718902.2:n.2179+13G=
XM_011542829.2:c.4795+13G=	XP_011541131.1:n.4795+13G=
XM_011542830.2:c.4792+13G=	XP_011541132.1:n.4792+13G=
XM_011542831.2:c.4795+13G=	XP_011541133.1:n.4795+13G=
XM_011542833.2:c.2278+13G=	XP_011541135.1:n.2278+13G=
NM_001197104.2:c.4696+13G= MANE Select	NP_001184033.1:n.4696+13G=
NM_005933.4:c.4696+13G=	NP_005924.2:n.4696+13G=