Canonical Allele Identifier: CA477091669

Gene: KMT2A

Linked Data

• gnomAD v4: 11-118491308-A-G
• MyVariant Identifiers: chr11:g.118362023A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118491308A>G , CM000673.2:g.118491308A>G	GRCh38
NC_000011.9:g.118362023A>G , CM000673.1:g.118362023A>G	GRCh37
NC_000011.8:g.117867233A>G	NCBI36
NG_027813.1:g.59819A>G , LRG_613:g.59819A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000531904.7:c.4908A>G	ENSP00000432391.3:p.Ser1636=
ENST00000710560.1:c.4908A>G	ENSP00000518343.1:p.Ser1636=
ENST00000685498.1:c.585A>G	ENSP00000509293.1:p.Ser195=
ENST00000691053.1:c.4809A>G	ENSP00000509168.1:p.Ser1603=
ENST00000389506.10:c.4809A>G	ENSP00000374157.5:p.Ser1603=
ENST00000534358.8:c.4809A>G MANE Select	ENSP00000436786.2:p.Ser1603=
ENST00000649699.1:c.4695A>G	ENSP00000496927.1:p.Ser1565=
ENST00000389506.9:c.4809A>G	ENSP00000374157.5:p.Ser1603=
ENST00000392873.3:c.945A>G	ENSP00000376612.3:p.Ser315=
ENST00000534358.5:c.4809A>G	ENSP00000436786.1:p.Ser1603=
NM_001197104.1:c.4809A>G , LRG_613t1:c.4809A>G	NP_001184033.1:p.Ser1603=
NM_005933.3:c.4809A>G	NP_005924.2:p.Ser1603=
XM_006718839.2:c.2292A>G	XP_006718902.2:p.Ser764=
XM_011542829.1:c.4908A>G	XP_011541131.1:p.Ser1636=
XM_011542830.1:c.4905A>G	XP_011541132.1:p.Ser1635=
XM_011542831.1:c.4908A>G	XP_011541133.1:p.Ser1636=
XM_011542832.1:c.2715A>G	XP_011541134.1:p.Ser905=
XM_011542833.1:c.2391A>G	XP_011541135.1:p.Ser797=
XM_006718839.3:c.2292A>G	XP_006718902.2:p.Ser764=
XM_011542829.2:c.4908A>G	XP_011541131.1:p.Ser1636=
XM_011542830.2:c.4905A>G	XP_011541132.1:p.Ser1635=
XM_011542831.2:c.4908A>G	XP_011541133.1:p.Ser1636=
XM_011542833.2:c.2391A>G	XP_011541135.1:p.Ser797=
NM_001197104.2:c.4809A>G MANE Select	NP_001184033.1:p.Ser1603=
NM_005933.4:c.4809A>G	NP_005924.2:p.Ser1603=