Canonical Allele Identifier: CA477359713

Gene: KMT2A

Linked Data

• MyVariant Identifiers: chr11:g.118374173A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118503458A>T , CM000673.2:g.118503458A>T	GRCh38
NC_000011.9:g.118374173A>T , CM000673.1:g.118374173A>T	GRCh37
NC_000011.8:g.117879383A>T	NCBI36
NG_027813.1:g.71969A>T , LRG_613:g.71969A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000531904.7:c.7665A>T	ENSP00000432391.3:p.Thr2555=
ENST00000710560.1:c.7656A>T	ENSP00000518343.1:p.Thr2552=
ENST00000649878.2:c.1605A>T	ENSP00000497891.2:p.Thr535=
ENST00000685397.1:c.1605A>T	ENSP00000509586.1:p.Thr535=
ENST00000686370.1:c.1605A>T	ENSP00000509179.1:p.Thr535=
ENST00000689424.1:c.1863A>T	ENSP00000509852.1:p.Thr621=
ENST00000691053.1:c.7638A>T	ENSP00000509168.1:p.Thr2546=
ENST00000389506.10:c.7557A>T	ENSP00000374157.5:p.Thr2519=
ENST00000528278.2:n.6908A>T
ENST00000534358.8:c.7566A>T MANE Select	ENSP00000436786.2:p.Thr2522=
ENST00000649699.1:c.7443A>T	ENSP00000496927.1:p.Thr2481=
ENST00000389506.9:c.7557A>T	ENSP00000374157.5:p.Thr2519=
ENST00000528278.1:n.1693A>T
ENST00000534358.5:c.7566A>T	ENSP00000436786.1:p.Thr2522=
NM_001197104.1:c.7566A>T , LRG_613t1:c.7566A>T	NP_001184033.1:p.Thr2522=
NM_005933.3:c.7557A>T	NP_005924.2:p.Thr2519=
XM_006718839.2:c.5049A>T	XP_006718902.2:p.Thr1683=
XM_011542829.1:c.7665A>T	XP_011541131.1:p.Thr2555=
XM_011542830.1:c.7662A>T	XP_011541132.1:p.Thr2554=
XM_011542831.1:c.7656A>T	XP_011541133.1:p.Thr2552=
XM_011542832.1:c.5472A>T	XP_011541134.1:p.Thr1824=
XM_011542833.1:c.5148A>T	XP_011541135.1:p.Thr1716=
XM_006718839.3:c.5049A>T	XP_006718902.2:p.Thr1683=
XM_011542829.2:c.7665A>T	XP_011541131.1:p.Thr2555=
XM_011542830.2:c.7662A>T	XP_011541132.1:p.Thr2554=
XM_011542831.2:c.7656A>T	XP_011541133.1:p.Thr2552=
XM_011542833.2:c.5148A>T	XP_011541135.1:p.Thr1716=
NM_001197104.2:c.7566A>T MANE Select	NP_001184033.1:p.Thr2522=
NM_005933.4:c.7557A>T	NP_005924.2:p.Thr2519=