Canonical Allele Identifier: CA382826534

Gene: KMT2A

Linked Data

• MyVariant Identifiers: chr11:g.118350944C>T (hg19) ; chr11:g.118480229C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118480229C>T , CM000673.2:g.118480229C>T	GRCh38
NC_000011.9:g.118350944C>T , CM000673.1:g.118350944C>T	GRCh37
NC_000011.8:g.117856154C>T	NCBI36
NG_027813.1:g.48740C>T , LRG_613:g.48740C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000531904.7:c.3724C>T	ENSP00000432391.3:p.Gln1242Ter
ENST00000710560.1:c.3724C>T	ENSP00000518343.1:p.Gln1242Ter
ENST00000527869.7:c.1207C>T	ENSP00000432652.3:p.Gln403Ter
ENST00000533790.3:c.1108C>T	ENSP00000436700.3:p.Gln370Ter
ENST00000649690.2:c.1432C>T	ENSP00000497372.2:p.Gln478Ter
ENST00000685719.1:c.606C>T
ENST00000691053.1:c.3625C>T	ENSP00000509168.1:p.Gln1209Ter
ENST00000389506.10:c.3625C>T	ENSP00000374157.5:p.Gln1209Ter
ENST00000533790.2:c.877C>T	ENSP00000436700.2:p.Gln293Ter
ENST00000534358.8:c.3625C>T MANE Select	ENSP00000436786.2:p.Gln1209Ter
ENST00000648261.1:c.2395C>T	ENSP00000498126.1:p.Gln799Ter
ENST00000649699.1:c.3625C>T	ENSP00000496927.1:p.Gln1209Ter
ENST00000389506.9:c.3625C>T	ENSP00000374157.5:p.Gln1209Ter
ENST00000531904.6:c.3724C>T	ENSP00000432391.2:p.Gln1242Ter
ENST00000534358.5:c.3625C>T	ENSP00000436786.1:p.Gln1209Ter
NM_001197104.1:c.3625C>T , LRG_613t1:c.3625C>T	NP_001184033.1:p.Gln1209Ter
NM_005933.3:c.3625C>T	NP_005924.2:p.Gln1209Ter
XM_006718839.2:c.1108C>T	XP_006718902.2:p.Gln370Ter
XM_011542829.1:c.3724C>T	XP_011541131.1:p.Gln1242Ter
XM_011542830.1:c.3724C>T	XP_011541132.1:p.Gln1242Ter
XM_011542831.1:c.3724C>T	XP_011541133.1:p.Gln1242Ter
XM_011542832.1:c.1531C>T	XP_011541134.1:p.Gln511Ter
XM_011542833.1:c.1207C>T	XP_011541135.1:p.Gln403Ter
XM_006718839.3:c.1108C>T	XP_006718902.2:p.Gln370Ter
XM_011542829.2:c.3724C>T	XP_011541131.1:p.Gln1242Ter
XM_011542830.2:c.3724C>T	XP_011541132.1:p.Gln1242Ter
XM_011542831.2:c.3724C>T	XP_011541133.1:p.Gln1242Ter
XM_011542833.2:c.1207C>T	XP_011541135.1:p.Gln403Ter
NM_001197104.2:c.3625C>T MANE Select	NP_001184033.1:p.Gln1209Ter
NM_005933.4:c.3625C>T	NP_005924.2:p.Gln1209Ter