Canonical Allele Identifier: CA382806238

Gene: KMT2A

Linked Data

• MyVariant Identifiers: chr11:g.118374231C>A (hg19) ; chr11:g.118503516C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118503516C>A , CM000673.2:g.118503516C>A	GRCh38
NC_000011.9:g.118374231C>A , CM000673.1:g.118374231C>A	GRCh37
NC_000011.8:g.117879441C>A	NCBI36
NG_027813.1:g.72027C>A , LRG_613:g.72027C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000531904.7:c.7723C>A	ENSP00000432391.3:p.Leu2575Met
ENST00000710560.1:c.7714C>A	ENSP00000518343.1:p.Leu2572Met
ENST00000649878.2:c.1663C>A	ENSP00000497891.2:p.Leu555Met
ENST00000685397.1:c.1663C>A	ENSP00000509586.1:p.Leu555Met
ENST00000686370.1:c.1663C>A	ENSP00000509179.1:p.Leu555Met
ENST00000689424.1:c.1921C>A	ENSP00000509852.1:p.Leu641Met
ENST00000691053.1:c.7696C>A	ENSP00000509168.1:p.Leu2566Met
ENST00000389506.10:c.7615C>A	ENSP00000374157.5:p.Leu2539Met
ENST00000528278.2:n.6966C>A
ENST00000534358.8:c.7624C>A MANE Select	ENSP00000436786.2:p.Leu2542Met
ENST00000649699.1:c.7501C>A	ENSP00000496927.1:p.Leu2501Met
ENST00000389506.9:c.7615C>A	ENSP00000374157.5:p.Leu2539Met
ENST00000528278.1:n.1751C>A
ENST00000534358.5:c.7624C>A	ENSP00000436786.1:p.Leu2542Met
NM_001197104.1:c.7624C>A , LRG_613t1:c.7624C>A	NP_001184033.1:p.Leu2542Met
NM_005933.3:c.7615C>A	NP_005924.2:p.Leu2539Met
XM_006718839.2:c.5107C>A	XP_006718902.2:p.Leu1703Met
XM_011542829.1:c.7723C>A	XP_011541131.1:p.Leu2575Met
XM_011542830.1:c.7720C>A	XP_011541132.1:p.Leu2574Met
XM_011542831.1:c.7714C>A	XP_011541133.1:p.Leu2572Met
XM_011542832.1:c.5530C>A	XP_011541134.1:p.Leu1844Met
XM_011542833.1:c.5206C>A	XP_011541135.1:p.Leu1736Met
XM_006718839.3:c.5107C>A	XP_006718902.2:p.Leu1703Met
XM_011542829.2:c.7723C>A	XP_011541131.1:p.Leu2575Met
XM_011542830.2:c.7720C>A	XP_011541132.1:p.Leu2574Met
XM_011542831.2:c.7714C>A	XP_011541133.1:p.Leu2572Met
XM_011542833.2:c.5206C>A	XP_011541135.1:p.Leu1736Met
NM_001197104.2:c.7624C>A MANE Select	NP_001184033.1:p.Leu2542Met
NM_005933.4:c.7615C>A	NP_005924.2:p.Leu2539Met