Canonical Allele Identifier: CA382802235

Gene: KMT2A

Linked Data

• MyVariant Identifiers: chr11:g.118373173G>A (hg19) ; chr11:g.118502458G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118502458G>A , CM000673.2:g.118502458G>A	GRCh38
NC_000011.9:g.118373173G>A , CM000673.1:g.118373173G>A	GRCh37
NC_000011.8:g.117878383G>A	NCBI36
NG_027813.1:g.70969G>A , LRG_613:g.70969G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000531904.7:c.6665G>A	ENSP00000432391.3:p.Gly2222Glu
ENST00000710560.1:c.6656G>A	ENSP00000518343.1:p.Gly2219Glu
ENST00000649878.2:c.605G>A	ENSP00000497891.2:p.Gly202Glu
ENST00000685397.1:c.605G>A	ENSP00000509586.1:p.Gly202Glu
ENST00000686370.1:c.605G>A	ENSP00000509179.1:p.Gly202Glu
ENST00000689424.1:c.863G>A	ENSP00000509852.1:p.Gly288Glu
ENST00000691053.1:c.6638G>A	ENSP00000509168.1:p.Gly2213Glu
ENST00000389506.10:c.6557G>A	ENSP00000374157.5:p.Gly2186Glu
ENST00000528278.2:n.5908G>A
ENST00000534358.8:c.6566G>A MANE Select	ENSP00000436786.2:p.Gly2189Glu
ENST00000649699.1:c.6443G>A	ENSP00000496927.1:p.Gly2148Glu
ENST00000389506.9:c.6557G>A	ENSP00000374157.5:p.Gly2186Glu
ENST00000528278.1:n.693G>A
ENST00000534358.5:c.6566G>A	ENSP00000436786.1:p.Gly2189Glu
NM_001197104.1:c.6566G>A , LRG_613t1:c.6566G>A	NP_001184033.1:p.Gly2189Glu
NM_005933.3:c.6557G>A	NP_005924.2:p.Gly2186Glu
XM_006718839.2:c.4049G>A	XP_006718902.2:p.Gly1350Glu
XM_011542829.1:c.6665G>A	XP_011541131.1:p.Gly2222Glu
XM_011542830.1:c.6662G>A	XP_011541132.1:p.Gly2221Glu
XM_011542831.1:c.6656G>A	XP_011541133.1:p.Gly2219Glu
XM_011542832.1:c.4472G>A	XP_011541134.1:p.Gly1491Glu
XM_011542833.1:c.4148G>A	XP_011541135.1:p.Gly1383Glu
XM_006718839.3:c.4049G>A	XP_006718902.2:p.Gly1350Glu
XM_011542829.2:c.6665G>A	XP_011541131.1:p.Gly2222Glu
XM_011542830.2:c.6662G>A	XP_011541132.1:p.Gly2221Glu
XM_011542831.2:c.6656G>A	XP_011541133.1:p.Gly2219Glu
XM_011542833.2:c.4148G>A	XP_011541135.1:p.Gly1383Glu
NM_001197104.2:c.6566G>A MANE Select	NP_001184033.1:p.Gly2189Glu
NM_005933.4:c.6557G>A	NP_005924.2:p.Gly2186Glu