Canonical Allele Identifier: CA382834269

Gene: KMT2A

Linked Data

• MyVariant Identifiers: chr11:g.118361925C>G (hg19) ; chr11:g.118491210C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118491210C>G , CM000673.2:g.118491210C>G	GRCh38
NC_000011.9:g.118361925C>G , CM000673.1:g.118361925C>G	GRCh37
NC_000011.8:g.117867135C>G	NCBI36
NG_027813.1:g.59721C>G , LRG_613:g.59721C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000531904.7:c.4810C>G	ENSP00000432391.3:p.Leu1604Val
ENST00000710560.1:c.4810C>G	ENSP00000518343.1:p.Leu1604Val
ENST00000685498.1:c.487C>G	ENSP00000509293.1:p.Leu163Val
ENST00000691053.1:c.4711C>G	ENSP00000509168.1:p.Leu1571Val
ENST00000389506.10:c.4711C>G	ENSP00000374157.5:p.Leu1571Val
ENST00000534358.8:c.4711C>G MANE Select	ENSP00000436786.2:p.Leu1571Val
ENST00000649699.1:c.4597C>G	ENSP00000496927.1:p.Leu1533Val
ENST00000389506.9:c.4711C>G	ENSP00000374157.5:p.Leu1571Val
ENST00000392873.3:c.847C>G	ENSP00000376612.3:p.Leu283Val
ENST00000534358.5:c.4711C>G	ENSP00000436786.1:p.Leu1571Val
NM_001197104.1:c.4711C>G , LRG_613t1:c.4711C>G	NP_001184033.1:p.Leu1571Val
NM_005933.3:c.4711C>G	NP_005924.2:p.Leu1571Val
XM_006718839.2:c.2194C>G	XP_006718902.2:p.Leu732Val
XM_011542829.1:c.4810C>G	XP_011541131.1:p.Leu1604Val
XM_011542830.1:c.4807C>G	XP_011541132.1:p.Leu1603Val
XM_011542831.1:c.4810C>G	XP_011541133.1:p.Leu1604Val
XM_011542832.1:c.2617C>G	XP_011541134.1:p.Leu873Val
XM_011542833.1:c.2293C>G	XP_011541135.1:p.Leu765Val
XM_006718839.3:c.2194C>G	XP_006718902.2:p.Leu732Val
XM_011542829.2:c.4810C>G	XP_011541131.1:p.Leu1604Val
XM_011542830.2:c.4807C>G	XP_011541132.1:p.Leu1603Val
XM_011542831.2:c.4810C>G	XP_011541133.1:p.Leu1604Val
XM_011542833.2:c.2293C>G	XP_011541135.1:p.Leu765Val
NM_001197104.2:c.4711C>G MANE Select	NP_001184033.1:p.Leu1571Val
NM_005933.4:c.4711C>G	NP_005924.2:p.Leu1571Val