Canonical Allele Identifier: CA477359431

Gene: KMT2A

Linked Data

• MyVariant Identifiers: chr11:g.118374045C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118503330C>A , CM000673.2:g.118503330C>A	GRCh38
NC_000011.9:g.118374045C>A , CM000673.1:g.118374045C>A	GRCh37
NC_000011.8:g.117879255C>A	NCBI36
NG_027813.1:g.71841C>A , LRG_613:g.71841C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000531904.7:c.7537C>A	ENSP00000432391.3:p.Arg2513=
ENST00000710560.1:c.7528C>A	ENSP00000518343.1:p.Arg2510=
ENST00000649878.2:c.1477C>A	ENSP00000497891.2:p.Arg493=
ENST00000685397.1:c.1477C>A	ENSP00000509586.1:p.Arg493=
ENST00000686370.1:c.1477C>A	ENSP00000509179.1:p.Arg493=
ENST00000689424.1:c.1735C>A	ENSP00000509852.1:p.Arg579=
ENST00000691053.1:c.7510C>A	ENSP00000509168.1:p.Arg2504=
ENST00000389506.10:c.7429C>A	ENSP00000374157.5:p.Arg2477=
ENST00000528278.2:n.6780C>A
ENST00000534358.8:c.7438C>A MANE Select	ENSP00000436786.2:p.Arg2480=
ENST00000649699.1:c.7315C>A	ENSP00000496927.1:p.Arg2439=
ENST00000389506.9:c.7429C>A	ENSP00000374157.5:p.Arg2477=
ENST00000528278.1:n.1565C>A
ENST00000534358.5:c.7438C>A	ENSP00000436786.1:p.Arg2480=
NM_001197104.1:c.7438C>A , LRG_613t1:c.7438C>A	NP_001184033.1:p.Arg2480=
NM_005933.3:c.7429C>A	NP_005924.2:p.Arg2477=
XM_006718839.2:c.4921C>A	XP_006718902.2:p.Arg1641=
XM_011542829.1:c.7537C>A	XP_011541131.1:p.Arg2513=
XM_011542830.1:c.7534C>A	XP_011541132.1:p.Arg2512=
XM_011542831.1:c.7528C>A	XP_011541133.1:p.Arg2510=
XM_011542832.1:c.5344C>A	XP_011541134.1:p.Arg1782=
XM_011542833.1:c.5020C>A	XP_011541135.1:p.Arg1674=
XM_006718839.3:c.4921C>A	XP_006718902.2:p.Arg1641=
XM_011542829.2:c.7537C>A	XP_011541131.1:p.Arg2513=
XM_011542830.2:c.7534C>A	XP_011541132.1:p.Arg2512=
XM_011542831.2:c.7528C>A	XP_011541133.1:p.Arg2510=
XM_011542833.2:c.5020C>A	XP_011541135.1:p.Arg1674=
NM_001197104.2:c.7438C>A MANE Select	NP_001184033.1:p.Arg2480=
NM_005933.4:c.7429C>A	NP_005924.2:p.Arg2477=