Canonical Allele Identifier: CA2695215651

Gene: KMT2A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118491226dup , CM000673.2:g.118491226dup	GRCh38
NC_000011.9:g.118361941dup , CM000673.1:g.118361941dup	GRCh37
NC_000011.8:g.117867151dup	NCBI36
NG_027813.1:g.59737dup , LRG_613:g.59737dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000531904.7:c.4826dup	ENSP00000432391.3:p.Tyr1609Ter
ENST00000710560.1:c.4826dup	ENSP00000518343.1:p.Tyr1609Ter
ENST00000685498.1:c.503dup	ENSP00000509293.1:p.Tyr168Ter
ENST00000691053.1:c.4727dup	ENSP00000509168.1:p.Tyr1576Ter
ENST00000389506.10:c.4727dup	ENSP00000374157.5:p.Tyr1576Ter
ENST00000534358.8:c.4727dup MANE Select	ENSP00000436786.2:p.Tyr1576Ter
ENST00000649699.1:c.4613dup	ENSP00000496927.1:p.Tyr1538Ter
ENST00000389506.9:c.4727dup	ENSP00000374157.5:p.Tyr1576Ter
ENST00000392873.3:c.863dup	ENSP00000376612.3:p.Tyr288Ter
ENST00000534358.5:c.4727dup	ENSP00000436786.1:p.Tyr1576Ter
NM_001197104.1:c.4727dup , LRG_613t1:c.4727dup	NP_001184033.1:p.Tyr1576Ter
NM_005933.3:c.4727dup	NP_005924.2:p.Tyr1576Ter
XM_006718839.2:c.2210dup	XP_006718902.2:p.Tyr737Ter
XM_011542829.1:c.4826dup	XP_011541131.1:p.Tyr1609Ter
XM_011542830.1:c.4823dup	XP_011541132.1:p.Tyr1608Ter
XM_011542831.1:c.4826dup	XP_011541133.1:p.Tyr1609Ter
XM_011542832.1:c.2633dup	XP_011541134.1:p.Tyr878Ter
XM_011542833.1:c.2309dup	XP_011541135.1:p.Tyr770Ter
XM_006718839.3:c.2210dup	XP_006718902.2:p.Tyr737Ter
XM_011542829.2:c.4826dup	XP_011541131.1:p.Tyr1609Ter
XM_011542830.2:c.4823dup	XP_011541132.1:p.Tyr1608Ter
XM_011542831.2:c.4826dup	XP_011541133.1:p.Tyr1609Ter
XM_011542833.2:c.2309dup	XP_011541135.1:p.Tyr770Ter
NM_001197104.2:c.4727dup MANE Select	NP_001184033.1:p.Tyr1576Ter
NM_005933.4:c.4727dup	NP_005924.2:p.Tyr1576Ter