Canonical Allele Identifier: CA382802311

Gene: KMT2A

Linked Data

• MyVariant Identifiers: chr11:g.118373194G>T (hg19) ; chr11:g.118502479G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118502479G>T , CM000673.2:g.118502479G>T	GRCh38
NC_000011.9:g.118373194G>T , CM000673.1:g.118373194G>T	GRCh37
NC_000011.8:g.117878404G>T	NCBI36
NG_027813.1:g.70990G>T , LRG_613:g.70990G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000531904.7:c.6686G>T	ENSP00000432391.3:p.Arg2229Met
ENST00000710560.1:c.6677G>T	ENSP00000518343.1:p.Arg2226Met
ENST00000649878.2:c.626G>T	ENSP00000497891.2:p.Arg209Met
ENST00000685397.1:c.626G>T	ENSP00000509586.1:p.Arg209Met
ENST00000686370.1:c.626G>T	ENSP00000509179.1:p.Arg209Met
ENST00000689424.1:c.884G>T	ENSP00000509852.1:p.Arg295Met
ENST00000691053.1:c.6659G>T	ENSP00000509168.1:p.Arg2220Met
ENST00000389506.10:c.6578G>T	ENSP00000374157.5:p.Arg2193Met
ENST00000528278.2:n.5929G>T
ENST00000534358.8:c.6587G>T MANE Select	ENSP00000436786.2:p.Arg2196Met
ENST00000649699.1:c.6464G>T	ENSP00000496927.1:p.Arg2155Met
ENST00000389506.9:c.6578G>T	ENSP00000374157.5:p.Arg2193Met
ENST00000528278.1:n.714G>T
ENST00000534358.5:c.6587G>T	ENSP00000436786.1:p.Arg2196Met
NM_001197104.1:c.6587G>T , LRG_613t1:c.6587G>T	NP_001184033.1:p.Arg2196Met
NM_005933.3:c.6578G>T	NP_005924.2:p.Arg2193Met
XM_006718839.2:c.4070G>T	XP_006718902.2:p.Arg1357Met
XM_011542829.1:c.6686G>T	XP_011541131.1:p.Arg2229Met
XM_011542830.1:c.6683G>T	XP_011541132.1:p.Arg2228Met
XM_011542831.1:c.6677G>T	XP_011541133.1:p.Arg2226Met
XM_011542832.1:c.4493G>T	XP_011541134.1:p.Arg1498Met
XM_011542833.1:c.4169G>T	XP_011541135.1:p.Arg1390Met
XM_006718839.3:c.4070G>T	XP_006718902.2:p.Arg1357Met
XM_011542829.2:c.6686G>T	XP_011541131.1:p.Arg2229Met
XM_011542830.2:c.6683G>T	XP_011541132.1:p.Arg2228Met
XM_011542831.2:c.6677G>T	XP_011541133.1:p.Arg2226Met
XM_011542833.2:c.4169G>T	XP_011541135.1:p.Arg1390Met
NM_001197104.2:c.6587G>T MANE Select	NP_001184033.1:p.Arg2196Met
NM_005933.4:c.6578G>T	NP_005924.2:p.Arg2193Met