Canonical Allele Identifier: CA382804873

Gene: KMT2A

Linked Data

• MyVariant Identifiers: chr11:g.118373868A>G (hg19) ; chr11:g.118503153A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118503153A>G , CM000673.2:g.118503153A>G	GRCh38
NC_000011.9:g.118373868A>G , CM000673.1:g.118373868A>G	GRCh37
NC_000011.8:g.117879078A>G	NCBI36
NG_027813.1:g.71664A>G , LRG_613:g.71664A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000531904.7:c.7360A>G	ENSP00000432391.3:p.Met2454Val
ENST00000710560.1:c.7351A>G	ENSP00000518343.1:p.Met2451Val
ENST00000649878.2:c.1300A>G	ENSP00000497891.2:p.Met434Val
ENST00000685397.1:c.1300A>G	ENSP00000509586.1:p.Met434Val
ENST00000686370.1:c.1300A>G	ENSP00000509179.1:p.Met434Val
ENST00000689424.1:c.1558A>G	ENSP00000509852.1:p.Met520Val
ENST00000691053.1:c.7333A>G	ENSP00000509168.1:p.Met2445Val
ENST00000389506.10:c.7252A>G	ENSP00000374157.5:p.Met2418Val
ENST00000528278.2:n.6603A>G
ENST00000534358.8:c.7261A>G MANE Select	ENSP00000436786.2:p.Met2421Val
ENST00000649699.1:c.7138A>G	ENSP00000496927.1:p.Met2380Val
ENST00000389506.9:c.7252A>G	ENSP00000374157.5:p.Met2418Val
ENST00000528278.1:n.1388A>G
ENST00000534358.5:c.7261A>G	ENSP00000436786.1:p.Met2421Val
NM_001197104.1:c.7261A>G , LRG_613t1:c.7261A>G	NP_001184033.1:p.Met2421Val
NM_005933.3:c.7252A>G	NP_005924.2:p.Met2418Val
XM_006718839.2:c.4744A>G	XP_006718902.2:p.Met1582Val
XM_011542829.1:c.7360A>G	XP_011541131.1:p.Met2454Val
XM_011542830.1:c.7357A>G	XP_011541132.1:p.Met2453Val
XM_011542831.1:c.7351A>G	XP_011541133.1:p.Met2451Val
XM_011542832.1:c.5167A>G	XP_011541134.1:p.Met1723Val
XM_011542833.1:c.4843A>G	XP_011541135.1:p.Met1615Val
XM_006718839.3:c.4744A>G	XP_006718902.2:p.Met1582Val
XM_011542829.2:c.7360A>G	XP_011541131.1:p.Met2454Val
XM_011542830.2:c.7357A>G	XP_011541132.1:p.Met2453Val
XM_011542831.2:c.7351A>G	XP_011541133.1:p.Met2451Val
XM_011542833.2:c.4843A>G	XP_011541135.1:p.Met1615Val
NM_001197104.2:c.7261A>G MANE Select	NP_001184033.1:p.Met2421Val
NM_005933.4:c.7252A>G	NP_005924.2:p.Met2418Val