Canonical Allele Identifier: CA477359244

Gene: KMT2A

Linked Data

• COSMIC: COSM5032099 ; COSM5032100
• MyVariant Identifiers: chr11:g.118373864A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118503149A>G , CM000673.2:g.118503149A>G	GRCh38
NC_000011.9:g.118373864A>G , CM000673.1:g.118373864A>G	GRCh37
NC_000011.8:g.117879074A>G	NCBI36
NG_027813.1:g.71660A>G , LRG_613:g.71660A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000531904.7:c.7356A>G	ENSP00000432391.3:p.Glu2452=
ENST00000710560.1:c.7347A>G	ENSP00000518343.1:p.Glu2449=
ENST00000649878.2:c.1296A>G	ENSP00000497891.2:p.Glu432=
ENST00000685397.1:c.1296A>G	ENSP00000509586.1:p.Glu432=
ENST00000686370.1:c.1296A>G	ENSP00000509179.1:p.Glu432=
ENST00000689424.1:c.1554A>G	ENSP00000509852.1:p.Glu518=
ENST00000691053.1:c.7329A>G	ENSP00000509168.1:p.Glu2443=
ENST00000389506.10:c.7248A>G	ENSP00000374157.5:p.Glu2416=
ENST00000528278.2:n.6599A>G
ENST00000534358.8:c.7257A>G MANE Select	ENSP00000436786.2:p.Glu2419=
ENST00000649699.1:c.7134A>G	ENSP00000496927.1:p.Glu2378=
ENST00000389506.9:c.7248A>G	ENSP00000374157.5:p.Glu2416=
ENST00000528278.1:n.1384A>G
ENST00000534358.5:c.7257A>G	ENSP00000436786.1:p.Glu2419=
NM_001197104.1:c.7257A>G , LRG_613t1:c.7257A>G	NP_001184033.1:p.Glu2419=
NM_005933.3:c.7248A>G	NP_005924.2:p.Glu2416=
XM_006718839.2:c.4740A>G	XP_006718902.2:p.Glu1580=
XM_011542829.1:c.7356A>G	XP_011541131.1:p.Glu2452=
XM_011542830.1:c.7353A>G	XP_011541132.1:p.Glu2451=
XM_011542831.1:c.7347A>G	XP_011541133.1:p.Glu2449=
XM_011542832.1:c.5163A>G	XP_011541134.1:p.Glu1721=
XM_011542833.1:c.4839A>G	XP_011541135.1:p.Glu1613=
XM_006718839.3:c.4740A>G	XP_006718902.2:p.Glu1580=
XM_011542829.2:c.7356A>G	XP_011541131.1:p.Glu2452=
XM_011542830.2:c.7353A>G	XP_011541132.1:p.Glu2451=
XM_011542831.2:c.7347A>G	XP_011541133.1:p.Glu2449=
XM_011542833.2:c.4839A>G	XP_011541135.1:p.Glu1613=
NM_001197104.2:c.7257A>G MANE Select	NP_001184033.1:p.Glu2419=
NM_005933.4:c.7248A>G	NP_005924.2:p.Glu2416=