Canonical Allele Identifier: CA477093576

Gene: KMT2A

Linked Data

• MyVariant Identifiers: chr11:g.118373345T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118502630T>A , CM000673.2:g.118502630T>A	GRCh38
NC_000011.9:g.118373345T>A , CM000673.1:g.118373345T>A	GRCh37
NC_000011.8:g.117878555T>A	NCBI36
NG_027813.1:g.71141T>A , LRG_613:g.71141T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000531904.7:c.6837T>A	ENSP00000432391.3:p.Val2279=
ENST00000710560.1:c.6828T>A	ENSP00000518343.1:p.Val2276=
ENST00000649878.2:c.777T>A	ENSP00000497891.2:p.Val259=
ENST00000685397.1:c.777T>A	ENSP00000509586.1:p.Val259=
ENST00000686370.1:c.777T>A	ENSP00000509179.1:p.Val259=
ENST00000689424.1:c.1035T>A	ENSP00000509852.1:p.Val345=
ENST00000691053.1:c.6810T>A	ENSP00000509168.1:p.Val2270=
ENST00000389506.10:c.6729T>A	ENSP00000374157.5:p.Val2243=
ENST00000528278.2:n.6080T>A
ENST00000534358.8:c.6738T>A MANE Select	ENSP00000436786.2:p.Val2246=
ENST00000649699.1:c.6615T>A	ENSP00000496927.1:p.Val2205=
ENST00000389506.9:c.6729T>A	ENSP00000374157.5:p.Val2243=
ENST00000528278.1:n.865T>A
ENST00000534358.5:c.6738T>A	ENSP00000436786.1:p.Val2246=
NM_001197104.1:c.6738T>A , LRG_613t1:c.6738T>A	NP_001184033.1:p.Val2246=
NM_005933.3:c.6729T>A	NP_005924.2:p.Val2243=
XM_006718839.2:c.4221T>A	XP_006718902.2:p.Val1407=
XM_011542829.1:c.6837T>A	XP_011541131.1:p.Val2279=
XM_011542830.1:c.6834T>A	XP_011541132.1:p.Val2278=
XM_011542831.1:c.6828T>A	XP_011541133.1:p.Val2276=
XM_011542832.1:c.4644T>A	XP_011541134.1:p.Val1548=
XM_011542833.1:c.4320T>A	XP_011541135.1:p.Val1440=
XM_006718839.3:c.4221T>A	XP_006718902.2:p.Val1407=
XM_011542829.2:c.6837T>A	XP_011541131.1:p.Val2279=
XM_011542830.2:c.6834T>A	XP_011541132.1:p.Val2278=
XM_011542831.2:c.6828T>A	XP_011541133.1:p.Val2276=
XM_011542833.2:c.4320T>A	XP_011541135.1:p.Val1440=
NM_001197104.2:c.6738T>A MANE Select	NP_001184033.1:p.Val2246=
NM_005933.4:c.6729T>A	NP_005924.2:p.Val2243=