Canonical Allele Identifier: CA477359313

Gene: KMT2A

Linked Data

• MyVariant Identifiers: chr11:g.118373924T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118503209T>G , CM000673.2:g.118503209T>G	GRCh38
NC_000011.9:g.118373924T>G , CM000673.1:g.118373924T>G	GRCh37
NC_000011.8:g.117879134T>G	NCBI36
NG_027813.1:g.71720T>G , LRG_613:g.71720T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000531904.7:c.7416T>G	ENSP00000432391.3:p.Thr2472=
ENST00000710560.1:c.7407T>G	ENSP00000518343.1:p.Thr2469=
ENST00000649878.2:c.1356T>G	ENSP00000497891.2:p.Thr452=
ENST00000685397.1:c.1356T>G	ENSP00000509586.1:p.Thr452=
ENST00000686370.1:c.1356T>G	ENSP00000509179.1:p.Thr452=
ENST00000689424.1:c.1614T>G	ENSP00000509852.1:p.Thr538=
ENST00000691053.1:c.7389T>G	ENSP00000509168.1:p.Thr2463=
ENST00000389506.10:c.7308T>G	ENSP00000374157.5:p.Thr2436=
ENST00000528278.2:n.6659T>G
ENST00000534358.8:c.7317T>G MANE Select	ENSP00000436786.2:p.Thr2439=
ENST00000649699.1:c.7194T>G	ENSP00000496927.1:p.Thr2398=
ENST00000389506.9:c.7308T>G	ENSP00000374157.5:p.Thr2436=
ENST00000528278.1:n.1444T>G
ENST00000534358.5:c.7317T>G	ENSP00000436786.1:p.Thr2439=
NM_001197104.1:c.7317T>G , LRG_613t1:c.7317T>G	NP_001184033.1:p.Thr2439=
NM_005933.3:c.7308T>G	NP_005924.2:p.Thr2436=
XM_006718839.2:c.4800T>G	XP_006718902.2:p.Thr1600=
XM_011542829.1:c.7416T>G	XP_011541131.1:p.Thr2472=
XM_011542830.1:c.7413T>G	XP_011541132.1:p.Thr2471=
XM_011542831.1:c.7407T>G	XP_011541133.1:p.Thr2469=
XM_011542832.1:c.5223T>G	XP_011541134.1:p.Thr1741=
XM_011542833.1:c.4899T>G	XP_011541135.1:p.Thr1633=
XM_006718839.3:c.4800T>G	XP_006718902.2:p.Thr1600=
XM_011542829.2:c.7416T>G	XP_011541131.1:p.Thr2472=
XM_011542830.2:c.7413T>G	XP_011541132.1:p.Thr2471=
XM_011542831.2:c.7407T>G	XP_011541133.1:p.Thr2469=
XM_011542833.2:c.4899T>G	XP_011541135.1:p.Thr1633=
NM_001197104.2:c.7317T>G MANE Select	NP_001184033.1:p.Thr2439=
NM_005933.4:c.7308T>G	NP_005924.2:p.Thr2436=