Canonical Allele Identifier: CA2725072497

Gene: KMT2A

Linked Data

• dbSNP Id: rs2134339586

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118491383_118491384insTTTCTCAGTGAT , CM000673.2:g.118491383_118491384insTTTCTCAGTGAT	GRCh38
NC_000011.9:g.118362098_118362099insTTTCTCAGTGAT , CM000673.1:g.118362098_118362099insTTTCTCAGTGAT	GRCh37
NC_000011.8:g.117867308_117867309insTTTCTCAGTGAT	NCBI36
NG_027813.1:g.59894_59895insTTTCTCAGTGAT , LRG_613:g.59894_59895insTTTCTCAGTGAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000531904.7:c.4918+65_4918+66insTTTCTCAGTGAT	ENSP00000432391.3:n.4918+65_4918+66insTTTCTCAGTGAT
ENST00000710560.1:c.4909+74_4909+75insTTTCTCAGTGAT	ENSP00000518343.1:n.4909+74_4909+75insTTTCTCAGTGAT
ENST00000685498.1:c.595+65_595+66insTTTCTCAGTGAT	ENSP00000509293.1:n.595+65_595+66insTTTCTCAGTGAT
ENST00000691053.1:c.4810+74_4810+75insTTTCTCAGTGAT	ENSP00000509168.1:n.4810+74_4810+75insTTTCTCAGTGAT
ENST00000389506.10:c.4810+74_4810+75insTTTCTCAGTGAT	ENSP00000374157.5:n.4810+74_4810+75insTTTCTCAGTGAT
ENST00000534358.8:c.4819+65_4819+66insTTTCTCAGTGAT MANE Select	ENSP00000436786.2:n.4819+65_4819+66insTTTCTCAGTGAT
ENST00000649699.1:c.4696+74_4696+75insTTTCTCAGTGAT	ENSP00000496927.1:n.4696+74_4696+75insTTTCTCAGTGAT
ENST00000389506.9:c.4810+74_4810+75insTTTCTCAGTGAT	ENSP00000374157.5:n.4810+74_4810+75insTTTCTCAGTGAT
ENST00000392873.3:c.946+74_946+75insTTTCTCAGTGAT	ENSP00000376612.3:n.946+74_946+75insTTTCTCAGTGAT
ENST00000534358.5:c.4819+65_4819+66insTTTCTCAGTGAT	ENSP00000436786.1:n.4819+65_4819+66insTTTCTCAGTGAT
NM_001197104.1:c.4819+65_4819+66insTTTCTCAGTGAT , LRG_613t1:c.4819+65_4819+66insTTTCTCAGTGAT	NP_001184033.1:n.4819+65_4819+66insTTTCTCAGTGAT
NM_005933.3:c.4810+74_4810+75insTTTCTCAGTGAT	NP_005924.2:n.4810+74_4810+75insTTTCTCAGTGAT
XM_006718839.2:c.2302+65_2302+66insTTTCTCAGTGAT	XP_006718902.2:n.2302+65_2302+66insTTTCTCAGTGAT
XM_011542829.1:c.4918+65_4918+66insTTTCTCAGTGAT	XP_011541131.1:n.4918+65_4918+66insTTTCTCAGTGAT
XM_011542830.1:c.4915+65_4915+66insTTTCTCAGTGAT	XP_011541132.1:n.4915+65_4915+66insTTTCTCAGTGAT
XM_011542831.1:c.4909+74_4909+75insTTTCTCAGTGAT	XP_011541133.1:n.4909+74_4909+75insTTTCTCAGTGAT
XM_011542832.1:c.2725+65_2725+66insTTTCTCAGTGAT	XP_011541134.1:n.2725+65_2725+66insTTTCTCAGTGAT
XM_011542833.1:c.2401+65_2401+66insTTTCTCAGTGAT	XP_011541135.1:n.2401+65_2401+66insTTTCTCAGTGAT
XM_006718839.3:c.2302+65_2302+66insTTTCTCAGTGAT	XP_006718902.2:n.2302+65_2302+66insTTTCTCAGTGAT
XM_011542829.2:c.4918+65_4918+66insTTTCTCAGTGAT	XP_011541131.1:n.4918+65_4918+66insTTTCTCAGTGAT
XM_011542830.2:c.4915+65_4915+66insTTTCTCAGTGAT	XP_011541132.1:n.4915+65_4915+66insTTTCTCAGTGAT
XM_011542831.2:c.4909+74_4909+75insTTTCTCAGTGAT	XP_011541133.1:n.4909+74_4909+75insTTTCTCAGTGAT
XM_011542833.2:c.2401+65_2401+66insTTTCTCAGTGAT	XP_011541135.1:n.2401+65_2401+66insTTTCTCAGTGAT
NM_001197104.2:c.4819+65_4819+66insTTTCTCAGTGAT MANE Select	NP_001184033.1:n.4819+65_4819+66insTTTCTCAGTGAT
NM_005933.4:c.4810+74_4810+75insTTTCTCAGTGAT	NP_005924.2:n.4810+74_4810+75insTTTCTCAGTGAT