Canonical Allele Identifier: CA382832709

Gene: KMT2A

Linked Data

• MyVariant Identifiers: chr11:g.118359437T>G (hg19) ; chr11:g.118488722T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118488722T>G , CM000673.2:g.118488722T>G	GRCh38
NC_000011.9:g.118359437T>G , CM000673.1:g.118359437T>G	GRCh37
NC_000011.8:g.117864647T>G	NCBI36
NG_027813.1:g.57233T>G , LRG_613:g.57233T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000531904.7:c.4540T>G	ENSP00000432391.3:p.Phe1514Val
ENST00000710560.1:c.4540T>G	ENSP00000518343.1:p.Phe1514Val
ENST00000420751.4:c.352T>G	ENSP00000510776.1:p.Phe118Val
ENST00000685498.1:c.220T>G	ENSP00000509293.1:p.Phe74Val
ENST00000691053.1:c.4441T>G	ENSP00000509168.1:p.Phe1481Val
ENST00000389506.10:c.4441T>G	ENSP00000374157.5:p.Phe1481Val
ENST00000534358.8:c.4441T>G MANE Select	ENSP00000436786.2:p.Phe1481Val
ENST00000649699.1:c.4327T>G	ENSP00000496927.1:p.Phe1443Val
ENST00000389506.9:c.4441T>G	ENSP00000374157.5:p.Phe1481Val
ENST00000392873.3:c.577T>G	ENSP00000376612.3:p.Phe193Val
ENST00000534358.5:c.4441T>G	ENSP00000436786.1:p.Phe1481Val
NM_001197104.1:c.4441T>G , LRG_613t1:c.4441T>G	NP_001184033.1:p.Phe1481Val
NM_005933.3:c.4441T>G	NP_005924.2:p.Phe1481Val
XM_006718839.2:c.1924T>G	XP_006718902.2:p.Phe642Val
XM_011542829.1:c.4540T>G	XP_011541131.1:p.Phe1514Val
XM_011542830.1:c.4540T>G	XP_011541132.1:p.Phe1514Val
XM_011542831.1:c.4540T>G	XP_011541133.1:p.Phe1514Val
XM_011542832.1:c.2347T>G	XP_011541134.1:p.Phe783Val
XM_011542833.1:c.2023T>G	XP_011541135.1:p.Phe675Val
XM_006718839.3:c.1924T>G	XP_006718902.2:p.Phe642Val
XM_011542829.2:c.4540T>G	XP_011541131.1:p.Phe1514Val
XM_011542830.2:c.4540T>G	XP_011541132.1:p.Phe1514Val
XM_011542831.2:c.4540T>G	XP_011541133.1:p.Phe1514Val
XM_011542833.2:c.2023T>G	XP_011541135.1:p.Phe675Val
NM_001197104.2:c.4441T>G MANE Select	NP_001184033.1:p.Phe1481Val
NM_005933.4:c.4441T>G	NP_005924.2:p.Phe1481Val