Canonical Allele Identifier: CA382805461

Gene: KMT2A

Linked Data

• MyVariant Identifiers: chr11:g.118374016A>T (hg19) ; chr11:g.118503301A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118503301A>T , CM000673.2:g.118503301A>T	GRCh38
NC_000011.9:g.118374016A>T , CM000673.1:g.118374016A>T	GRCh37
NC_000011.8:g.117879226A>T	NCBI36
NG_027813.1:g.71812A>T , LRG_613:g.71812A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000531904.7:c.7508A>T	ENSP00000432391.3:p.Glu2503Val
ENST00000710560.1:c.7499A>T	ENSP00000518343.1:p.Glu2500Val
ENST00000649878.2:c.1448A>T	ENSP00000497891.2:p.Glu483Val
ENST00000685397.1:c.1448A>T	ENSP00000509586.1:p.Glu483Val
ENST00000686370.1:c.1448A>T	ENSP00000509179.1:p.Glu483Val
ENST00000689424.1:c.1706A>T	ENSP00000509852.1:p.Glu569Val
ENST00000691053.1:c.7481A>T	ENSP00000509168.1:p.Glu2494Val
ENST00000389506.10:c.7400A>T	ENSP00000374157.5:p.Glu2467Val
ENST00000528278.2:n.6751A>T
ENST00000534358.8:c.7409A>T MANE Select	ENSP00000436786.2:p.Glu2470Val
ENST00000649699.1:c.7286A>T	ENSP00000496927.1:p.Glu2429Val
ENST00000389506.9:c.7400A>T	ENSP00000374157.5:p.Glu2467Val
ENST00000528278.1:n.1536A>T
ENST00000534358.5:c.7409A>T	ENSP00000436786.1:p.Glu2470Val
NM_001197104.1:c.7409A>T , LRG_613t1:c.7409A>T	NP_001184033.1:p.Glu2470Val
NM_005933.3:c.7400A>T	NP_005924.2:p.Glu2467Val
XM_006718839.2:c.4892A>T	XP_006718902.2:p.Glu1631Val
XM_011542829.1:c.7508A>T	XP_011541131.1:p.Glu2503Val
XM_011542830.1:c.7505A>T	XP_011541132.1:p.Glu2502Val
XM_011542831.1:c.7499A>T	XP_011541133.1:p.Glu2500Val
XM_011542832.1:c.5315A>T	XP_011541134.1:p.Glu1772Val
XM_011542833.1:c.4991A>T	XP_011541135.1:p.Glu1664Val
XM_006718839.3:c.4892A>T	XP_006718902.2:p.Glu1631Val
XM_011542829.2:c.7508A>T	XP_011541131.1:p.Glu2503Val
XM_011542830.2:c.7505A>T	XP_011541132.1:p.Glu2502Val
XM_011542831.2:c.7499A>T	XP_011541133.1:p.Glu2500Val
XM_011542833.2:c.4991A>T	XP_011541135.1:p.Glu1664Val
NM_001197104.2:c.7409A>T MANE Select	NP_001184033.1:p.Glu2470Val
NM_005933.4:c.7400A>T	NP_005924.2:p.Glu2467Val