Canonical Allele Identifier: CA382804960

Gene: KMT2A

Linked Data

• MyVariant Identifiers: chr11:g.118373892A>G (hg19) ; chr11:g.118503177A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118503177A>G , CM000673.2:g.118503177A>G	GRCh38
NC_000011.9:g.118373892A>G , CM000673.1:g.118373892A>G	GRCh37
NC_000011.8:g.117879102A>G	NCBI36
NG_027813.1:g.71688A>G , LRG_613:g.71688A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000531904.7:c.7384A>G	ENSP00000432391.3:p.Arg2462Gly
ENST00000710560.1:c.7375A>G	ENSP00000518343.1:p.Arg2459Gly
ENST00000649878.2:c.1324A>G	ENSP00000497891.2:p.Arg442Gly
ENST00000685397.1:c.1324A>G	ENSP00000509586.1:p.Arg442Gly
ENST00000686370.1:c.1324A>G	ENSP00000509179.1:p.Arg442Gly
ENST00000689424.1:c.1582A>G	ENSP00000509852.1:p.Arg528Gly
ENST00000691053.1:c.7357A>G	ENSP00000509168.1:p.Arg2453Gly
ENST00000389506.10:c.7276A>G	ENSP00000374157.5:p.Arg2426Gly
ENST00000528278.2:n.6627A>G
ENST00000534358.8:c.7285A>G MANE Select	ENSP00000436786.2:p.Arg2429Gly
ENST00000649699.1:c.7162A>G	ENSP00000496927.1:p.Arg2388Gly
ENST00000389506.9:c.7276A>G	ENSP00000374157.5:p.Arg2426Gly
ENST00000528278.1:n.1412A>G
ENST00000534358.5:c.7285A>G	ENSP00000436786.1:p.Arg2429Gly
NM_001197104.1:c.7285A>G , LRG_613t1:c.7285A>G	NP_001184033.1:p.Arg2429Gly
NM_005933.3:c.7276A>G	NP_005924.2:p.Arg2426Gly
XM_006718839.2:c.4768A>G	XP_006718902.2:p.Arg1590Gly
XM_011542829.1:c.7384A>G	XP_011541131.1:p.Arg2462Gly
XM_011542830.1:c.7381A>G	XP_011541132.1:p.Arg2461Gly
XM_011542831.1:c.7375A>G	XP_011541133.1:p.Arg2459Gly
XM_011542832.1:c.5191A>G	XP_011541134.1:p.Arg1731Gly
XM_011542833.1:c.4867A>G	XP_011541135.1:p.Arg1623Gly
XM_006718839.3:c.4768A>G	XP_006718902.2:p.Arg1590Gly
XM_011542829.2:c.7384A>G	XP_011541131.1:p.Arg2462Gly
XM_011542830.2:c.7381A>G	XP_011541132.1:p.Arg2461Gly
XM_011542831.2:c.7375A>G	XP_011541133.1:p.Arg2459Gly
XM_011542833.2:c.4867A>G	XP_011541135.1:p.Arg1623Gly
NM_001197104.2:c.7285A>G MANE Select	NP_001184033.1:p.Arg2429Gly
NM_005933.4:c.7276A>G	NP_005924.2:p.Arg2426Gly