Canonical Allele Identifier: CA382806385

Gene: KMT2A

Linked Data

• MyVariant Identifiers: chr11:g.118374268A>G (hg19) ; chr11:g.118503553A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118503553A>G , CM000673.2:g.118503553A>G	GRCh38
NC_000011.9:g.118374268A>G , CM000673.1:g.118374268A>G	GRCh37
NC_000011.8:g.117879478A>G	NCBI36
NG_027813.1:g.72064A>G , LRG_613:g.72064A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000531904.7:c.7760A>G	ENSP00000432391.3:p.Glu2587Gly
ENST00000710560.1:c.7751A>G	ENSP00000518343.1:p.Glu2584Gly
ENST00000649878.2:c.1700A>G	ENSP00000497891.2:p.Glu567Gly
ENST00000685397.1:c.1700A>G	ENSP00000509586.1:p.Glu567Gly
ENST00000686370.1:c.1700A>G	ENSP00000509179.1:p.Glu567Gly
ENST00000689424.1:c.1958A>G	ENSP00000509852.1:p.Glu653Gly
ENST00000691053.1:c.7733A>G	ENSP00000509168.1:p.Glu2578Gly
ENST00000389506.10:c.7652A>G	ENSP00000374157.5:p.Glu2551Gly
ENST00000528278.2:n.7003A>G
ENST00000534358.8:c.7661A>G MANE Select	ENSP00000436786.2:p.Glu2554Gly
ENST00000649699.1:c.7538A>G	ENSP00000496927.1:p.Glu2513Gly
ENST00000389506.9:c.7652A>G	ENSP00000374157.5:p.Glu2551Gly
ENST00000528278.1:n.1788A>G
ENST00000534358.5:c.7661A>G	ENSP00000436786.1:p.Glu2554Gly
NM_001197104.1:c.7661A>G , LRG_613t1:c.7661A>G	NP_001184033.1:p.Glu2554Gly
NM_005933.3:c.7652A>G	NP_005924.2:p.Glu2551Gly
XM_006718839.2:c.5144A>G	XP_006718902.2:p.Glu1715Gly
XM_011542829.1:c.7760A>G	XP_011541131.1:p.Glu2587Gly
XM_011542830.1:c.7757A>G	XP_011541132.1:p.Glu2586Gly
XM_011542831.1:c.7751A>G	XP_011541133.1:p.Glu2584Gly
XM_011542832.1:c.5567A>G	XP_011541134.1:p.Glu1856Gly
XM_011542833.1:c.5243A>G	XP_011541135.1:p.Glu1748Gly
XM_006718839.3:c.5144A>G	XP_006718902.2:p.Glu1715Gly
XM_011542829.2:c.7760A>G	XP_011541131.1:p.Glu2587Gly
XM_011542830.2:c.7757A>G	XP_011541132.1:p.Glu2586Gly
XM_011542831.2:c.7751A>G	XP_011541133.1:p.Glu2584Gly
XM_011542833.2:c.5243A>G	XP_011541135.1:p.Glu1748Gly
NM_001197104.2:c.7661A>G MANE Select	NP_001184033.1:p.Glu2554Gly
NM_005933.4:c.7652A>G	NP_005924.2:p.Glu2551Gly