Canonical Allele Identifier: CA477093519

Gene: KMT2A

Linked Data

• MyVariant Identifiers: chr11:g.118373270T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118502555T>A , CM000673.2:g.118502555T>A	GRCh38
NC_000011.9:g.118373270T>A , CM000673.1:g.118373270T>A	GRCh37
NC_000011.8:g.117878480T>A	NCBI36
NG_027813.1:g.71066T>A , LRG_613:g.71066T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000531904.7:c.6762T>A	ENSP00000432391.3:p.Thr2254=
ENST00000710560.1:c.6753T>A	ENSP00000518343.1:p.Thr2251=
ENST00000649878.2:c.702T>A	ENSP00000497891.2:p.Thr234=
ENST00000685397.1:c.702T>A	ENSP00000509586.1:p.Thr234=
ENST00000686370.1:c.702T>A	ENSP00000509179.1:p.Thr234=
ENST00000689424.1:c.960T>A	ENSP00000509852.1:p.Thr320=
ENST00000691053.1:c.6735T>A	ENSP00000509168.1:p.Thr2245=
ENST00000389506.10:c.6654T>A	ENSP00000374157.5:p.Thr2218=
ENST00000528278.2:n.6005T>A
ENST00000534358.8:c.6663T>A MANE Select	ENSP00000436786.2:p.Thr2221=
ENST00000649699.1:c.6540T>A	ENSP00000496927.1:p.Thr2180=
ENST00000389506.9:c.6654T>A	ENSP00000374157.5:p.Thr2218=
ENST00000528278.1:n.790T>A
ENST00000534358.5:c.6663T>A	ENSP00000436786.1:p.Thr2221=
NM_001197104.1:c.6663T>A , LRG_613t1:c.6663T>A	NP_001184033.1:p.Thr2221=
NM_005933.3:c.6654T>A	NP_005924.2:p.Thr2218=
XM_006718839.2:c.4146T>A	XP_006718902.2:p.Thr1382=
XM_011542829.1:c.6762T>A	XP_011541131.1:p.Thr2254=
XM_011542830.1:c.6759T>A	XP_011541132.1:p.Thr2253=
XM_011542831.1:c.6753T>A	XP_011541133.1:p.Thr2251=
XM_011542832.1:c.4569T>A	XP_011541134.1:p.Thr1523=
XM_011542833.1:c.4245T>A	XP_011541135.1:p.Thr1415=
XM_006718839.3:c.4146T>A	XP_006718902.2:p.Thr1382=
XM_011542829.2:c.6762T>A	XP_011541131.1:p.Thr2254=
XM_011542830.2:c.6759T>A	XP_011541132.1:p.Thr2253=
XM_011542831.2:c.6753T>A	XP_011541133.1:p.Thr2251=
XM_011542833.2:c.4245T>A	XP_011541135.1:p.Thr1415=
NM_001197104.2:c.6663T>A MANE Select	NP_001184033.1:p.Thr2221=
NM_005933.4:c.6654T>A	NP_005924.2:p.Thr2218=