Canonical Allele Identifier: CA477359626

Gene: KMT2A

Linked Data

• MyVariant Identifiers: chr11:g.118374131A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118503416A>T , CM000673.2:g.118503416A>T	GRCh38
NC_000011.9:g.118374131A>T , CM000673.1:g.118374131A>T	GRCh37
NC_000011.8:g.117879341A>T	NCBI36
NG_027813.1:g.71927A>T , LRG_613:g.71927A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000531904.7:c.7623A>T	ENSP00000432391.3:p.Val2541=
ENST00000710560.1:c.7614A>T	ENSP00000518343.1:p.Val2538=
ENST00000649878.2:c.1563A>T	ENSP00000497891.2:p.Val521=
ENST00000685397.1:c.1563A>T	ENSP00000509586.1:p.Val521=
ENST00000686370.1:c.1563A>T	ENSP00000509179.1:p.Val521=
ENST00000689424.1:c.1821A>T	ENSP00000509852.1:p.Val607=
ENST00000691053.1:c.7596A>T	ENSP00000509168.1:p.Val2532=
ENST00000389506.10:c.7515A>T	ENSP00000374157.5:p.Val2505=
ENST00000528278.2:n.6866A>T
ENST00000534358.8:c.7524A>T MANE Select	ENSP00000436786.2:p.Val2508=
ENST00000649699.1:c.7401A>T	ENSP00000496927.1:p.Val2467=
ENST00000389506.9:c.7515A>T	ENSP00000374157.5:p.Val2505=
ENST00000528278.1:n.1651A>T
ENST00000534358.5:c.7524A>T	ENSP00000436786.1:p.Val2508=
NM_001197104.1:c.7524A>T , LRG_613t1:c.7524A>T	NP_001184033.1:p.Val2508=
NM_005933.3:c.7515A>T	NP_005924.2:p.Val2505=
XM_006718839.2:c.5007A>T	XP_006718902.2:p.Val1669=
XM_011542829.1:c.7623A>T	XP_011541131.1:p.Val2541=
XM_011542830.1:c.7620A>T	XP_011541132.1:p.Val2540=
XM_011542831.1:c.7614A>T	XP_011541133.1:p.Val2538=
XM_011542832.1:c.5430A>T	XP_011541134.1:p.Val1810=
XM_011542833.1:c.5106A>T	XP_011541135.1:p.Val1702=
XM_006718839.3:c.5007A>T	XP_006718902.2:p.Val1669=
XM_011542829.2:c.7623A>T	XP_011541131.1:p.Val2541=
XM_011542830.2:c.7620A>T	XP_011541132.1:p.Val2540=
XM_011542831.2:c.7614A>T	XP_011541133.1:p.Val2538=
XM_011542833.2:c.5106A>T	XP_011541135.1:p.Val1702=
NM_001197104.2:c.7524A>T MANE Select	NP_001184033.1:p.Val2508=
NM_005933.4:c.7515A>T	NP_005924.2:p.Val2505=