Canonical Allele Identifier: CA382802255

Gene: KMT2A

Linked Data

• MyVariant Identifiers: chr11:g.118373181A>T (hg19) ; chr11:g.118502466A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118502466A>T , CM000673.2:g.118502466A>T	GRCh38
NC_000011.9:g.118373181A>T , CM000673.1:g.118373181A>T	GRCh37
NC_000011.8:g.117878391A>T	NCBI36
NG_027813.1:g.70977A>T , LRG_613:g.70977A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000531904.7:c.6673A>T	ENSP00000432391.3:p.Ser2225Cys
ENST00000710560.1:c.6664A>T	ENSP00000518343.1:p.Ser2222Cys
ENST00000649878.2:c.613A>T	ENSP00000497891.2:p.Ser205Cys
ENST00000685397.1:c.613A>T	ENSP00000509586.1:p.Ser205Cys
ENST00000686370.1:c.613A>T	ENSP00000509179.1:p.Ser205Cys
ENST00000689424.1:c.871A>T	ENSP00000509852.1:p.Ser291Cys
ENST00000691053.1:c.6646A>T	ENSP00000509168.1:p.Ser2216Cys
ENST00000389506.10:c.6565A>T	ENSP00000374157.5:p.Ser2189Cys
ENST00000528278.2:n.5916A>T
ENST00000534358.8:c.6574A>T MANE Select	ENSP00000436786.2:p.Ser2192Cys
ENST00000649699.1:c.6451A>T	ENSP00000496927.1:p.Ser2151Cys
ENST00000389506.9:c.6565A>T	ENSP00000374157.5:p.Ser2189Cys
ENST00000528278.1:n.701A>T
ENST00000534358.5:c.6574A>T	ENSP00000436786.1:p.Ser2192Cys
NM_001197104.1:c.6574A>T , LRG_613t1:c.6574A>T	NP_001184033.1:p.Ser2192Cys
NM_005933.3:c.6565A>T	NP_005924.2:p.Ser2189Cys
XM_006718839.2:c.4057A>T	XP_006718902.2:p.Ser1353Cys
XM_011542829.1:c.6673A>T	XP_011541131.1:p.Ser2225Cys
XM_011542830.1:c.6670A>T	XP_011541132.1:p.Ser2224Cys
XM_011542831.1:c.6664A>T	XP_011541133.1:p.Ser2222Cys
XM_011542832.1:c.4480A>T	XP_011541134.1:p.Ser1494Cys
XM_011542833.1:c.4156A>T	XP_011541135.1:p.Ser1386Cys
XM_006718839.3:c.4057A>T	XP_006718902.2:p.Ser1353Cys
XM_011542829.2:c.6673A>T	XP_011541131.1:p.Ser2225Cys
XM_011542830.2:c.6670A>T	XP_011541132.1:p.Ser2224Cys
XM_011542831.2:c.6664A>T	XP_011541133.1:p.Ser2222Cys
XM_011542833.2:c.4156A>T	XP_011541135.1:p.Ser1386Cys
NM_001197104.2:c.6574A>T MANE Select	NP_001184033.1:p.Ser2192Cys
NM_005933.4:c.6565A>T	NP_005924.2:p.Ser2189Cys