Canonical Allele Identifier: CA382804952

Gene: KMT2A

Linked Data

• MyVariant Identifiers: chr11:g.118373890G>A (hg19) ; chr11:g.118503175G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118503175G>A , CM000673.2:g.118503175G>A	GRCh38
NC_000011.9:g.118373890G>A , CM000673.1:g.118373890G>A	GRCh37
NC_000011.8:g.117879100G>A	NCBI36
NG_027813.1:g.71686G>A , LRG_613:g.71686G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000531904.7:c.7382G>A	ENSP00000432391.3:p.Arg2461Lys
ENST00000710560.1:c.7373G>A	ENSP00000518343.1:p.Arg2458Lys
ENST00000649878.2:c.1322G>A	ENSP00000497891.2:p.Arg441Lys
ENST00000685397.1:c.1322G>A	ENSP00000509586.1:p.Arg441Lys
ENST00000686370.1:c.1322G>A	ENSP00000509179.1:p.Arg441Lys
ENST00000689424.1:c.1580G>A	ENSP00000509852.1:p.Arg527Lys
ENST00000691053.1:c.7355G>A	ENSP00000509168.1:p.Arg2452Lys
ENST00000389506.10:c.7274G>A	ENSP00000374157.5:p.Arg2425Lys
ENST00000528278.2:n.6625G>A
ENST00000534358.8:c.7283G>A MANE Select	ENSP00000436786.2:p.Arg2428Lys
ENST00000649699.1:c.7160G>A	ENSP00000496927.1:p.Arg2387Lys
ENST00000389506.9:c.7274G>A	ENSP00000374157.5:p.Arg2425Lys
ENST00000528278.1:n.1410G>A
ENST00000534358.5:c.7283G>A	ENSP00000436786.1:p.Arg2428Lys
NM_001197104.1:c.7283G>A , LRG_613t1:c.7283G>A	NP_001184033.1:p.Arg2428Lys
NM_005933.3:c.7274G>A	NP_005924.2:p.Arg2425Lys
XM_006718839.2:c.4766G>A	XP_006718902.2:p.Arg1589Lys
XM_011542829.1:c.7382G>A	XP_011541131.1:p.Arg2461Lys
XM_011542830.1:c.7379G>A	XP_011541132.1:p.Arg2460Lys
XM_011542831.1:c.7373G>A	XP_011541133.1:p.Arg2458Lys
XM_011542832.1:c.5189G>A	XP_011541134.1:p.Arg1730Lys
XM_011542833.1:c.4865G>A	XP_011541135.1:p.Arg1622Lys
XM_006718839.3:c.4766G>A	XP_006718902.2:p.Arg1589Lys
XM_011542829.2:c.7382G>A	XP_011541131.1:p.Arg2461Lys
XM_011542830.2:c.7379G>A	XP_011541132.1:p.Arg2460Lys
XM_011542831.2:c.7373G>A	XP_011541133.1:p.Arg2458Lys
XM_011542833.2:c.4865G>A	XP_011541135.1:p.Arg1622Lys
NM_001197104.2:c.7283G>A MANE Select	NP_001184033.1:p.Arg2428Lys
NM_005933.4:c.7274G>A	NP_005924.2:p.Arg2425Lys