Canonical Allele Identifier: CA382806465

Gene: KMT2A

Linked Data

• MyVariant Identifiers: chr11:g.118374277C>G (hg19) ; chr11:g.118503562C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118503562C>G , CM000673.2:g.118503562C>G	GRCh38
NC_000011.9:g.118374277C>G , CM000673.1:g.118374277C>G	GRCh37
NC_000011.8:g.117879487C>G	NCBI36
NG_027813.1:g.72073C>G , LRG_613:g.72073C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000531904.7:c.7769C>G	ENSP00000432391.3:p.Ser2590Cys
ENST00000710560.1:c.7760C>G	ENSP00000518343.1:p.Ser2587Cys
ENST00000649878.2:c.1709C>G	ENSP00000497891.2:p.Ser570Cys
ENST00000685397.1:c.1709C>G	ENSP00000509586.1:p.Ser570Cys
ENST00000686370.1:c.1709C>G	ENSP00000509179.1:p.Ser570Cys
ENST00000689424.1:c.1967C>G	ENSP00000509852.1:p.Ser656Cys
ENST00000691053.1:c.7742C>G	ENSP00000509168.1:p.Ser2581Cys
ENST00000389506.10:c.7661C>G	ENSP00000374157.5:p.Ser2554Cys
ENST00000528278.2:n.7012C>G
ENST00000534358.8:c.7670C>G MANE Select	ENSP00000436786.2:p.Ser2557Cys
ENST00000649699.1:c.7547C>G	ENSP00000496927.1:p.Ser2516Cys
ENST00000389506.9:c.7661C>G	ENSP00000374157.5:p.Ser2554Cys
ENST00000528278.1:n.1797C>G
ENST00000534358.5:c.7670C>G	ENSP00000436786.1:p.Ser2557Cys
NM_001197104.1:c.7670C>G , LRG_613t1:c.7670C>G	NP_001184033.1:p.Ser2557Cys
NM_005933.3:c.7661C>G	NP_005924.2:p.Ser2554Cys
XM_006718839.2:c.5153C>G	XP_006718902.2:p.Ser1718Cys
XM_011542829.1:c.7769C>G	XP_011541131.1:p.Ser2590Cys
XM_011542830.1:c.7766C>G	XP_011541132.1:p.Ser2589Cys
XM_011542831.1:c.7760C>G	XP_011541133.1:p.Ser2587Cys
XM_011542832.1:c.5576C>G	XP_011541134.1:p.Ser1859Cys
XM_011542833.1:c.5252C>G	XP_011541135.1:p.Ser1751Cys
XM_006718839.3:c.5153C>G	XP_006718902.2:p.Ser1718Cys
XM_011542829.2:c.7769C>G	XP_011541131.1:p.Ser2590Cys
XM_011542830.2:c.7766C>G	XP_011541132.1:p.Ser2589Cys
XM_011542831.2:c.7760C>G	XP_011541133.1:p.Ser2587Cys
XM_011542833.2:c.5252C>G	XP_011541135.1:p.Ser1751Cys
NM_001197104.2:c.7670C>G MANE Select	NP_001184033.1:p.Ser2557Cys
NM_005933.4:c.7661C>G	NP_005924.2:p.Ser2554Cys