Canonical Allele Identifier: CA477089530

Gene: KMT2A

Linked Data

• MyVariant Identifiers: chr11:g.118359346C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118488631C>G , CM000673.2:g.118488631C>G	GRCh38
NC_000011.9:g.118359346C>G , CM000673.1:g.118359346C>G	GRCh37
NC_000011.8:g.117864556C>G	NCBI36
NG_027813.1:g.57142C>G , LRG_613:g.57142C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000531904.7:c.4449C>G	ENSP00000432391.3:p.Val1483=
ENST00000710560.1:c.4449C>G	ENSP00000518343.1:p.Val1483=
ENST00000420751.4:c.261C>G	ENSP00000510776.1:p.Val87=
ENST00000685498.1:c.129C>G	ENSP00000509293.1:p.Val43=
ENST00000691053.1:c.4350C>G	ENSP00000509168.1:p.Val1450=
ENST00000389506.10:c.4350C>G	ENSP00000374157.5:p.Val1450=
ENST00000534358.8:c.4350C>G MANE Select	ENSP00000436786.2:p.Val1450=
ENST00000649699.1:c.4236C>G	ENSP00000496927.1:p.Val1412=
ENST00000389506.9:c.4350C>G	ENSP00000374157.5:p.Val1450=
ENST00000392873.3:c.486C>G	ENSP00000376612.3:p.Val162=
ENST00000534358.5:c.4350C>G	ENSP00000436786.1:p.Val1450=
NM_001197104.1:c.4350C>G , LRG_613t1:c.4350C>G	NP_001184033.1:p.Val1450=
NM_005933.3:c.4350C>G	NP_005924.2:p.Val1450=
XM_006718839.2:c.1833C>G	XP_006718902.2:p.Val611=
XM_011542829.1:c.4449C>G	XP_011541131.1:p.Val1483=
XM_011542830.1:c.4449C>G	XP_011541132.1:p.Val1483=
XM_011542831.1:c.4449C>G	XP_011541133.1:p.Val1483=
XM_011542832.1:c.2256C>G	XP_011541134.1:p.Val752=
XM_011542833.1:c.1932C>G	XP_011541135.1:p.Val644=
XM_006718839.3:c.1833C>G	XP_006718902.2:p.Val611=
XM_011542829.2:c.4449C>G	XP_011541131.1:p.Val1483=
XM_011542830.2:c.4449C>G	XP_011541132.1:p.Val1483=
XM_011542831.2:c.4449C>G	XP_011541133.1:p.Val1483=
XM_011542833.2:c.1932C>G	XP_011541135.1:p.Val644=
NM_001197104.2:c.4350C>G MANE Select	NP_001184033.1:p.Val1450=
NM_005933.4:c.4350C>G	NP_005924.2:p.Val1450=