Canonical Allele Identifier: CA2724977009

Gene: KMT2A

Linked Data

• dbSNP Id: rs1555042391

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118491233_118491238del , CM000673.2:g.118491233_118491238del	GRCh38
NC_000011.9:g.118361948_118361953del , CM000673.1:g.118361948_118361953del	GRCh37
NC_000011.8:g.117867158_117867163del	NCBI36
NG_027813.1:g.59744_59749del , LRG_613:g.59744_59749del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000531904.7:c.4833_4838del	ENSP00000432391.3:p.Asp1612_Asp1613del
ENST00000710560.1:c.4833_4838del	ENSP00000518343.1:p.Asp1612_Asp1613del
ENST00000685498.1:c.510_515del	ENSP00000509293.1:p.Asp171_Asp172del
ENST00000691053.1:c.4734_4739del	ENSP00000509168.1:p.Asp1579_Asp1580del
ENST00000389506.10:c.4734_4739del	ENSP00000374157.5:p.Asp1579_Asp1580del
ENST00000534358.8:c.4734_4739del MANE Select	ENSP00000436786.2:p.Asp1579_Asp1580del
ENST00000649699.1:c.4620_4625del	ENSP00000496927.1:p.Asp1541_Asp1542del
ENST00000389506.9:c.4734_4739del	ENSP00000374157.5:p.Asp1579_Asp1580del
ENST00000392873.3:c.870_875del	ENSP00000376612.3:p.Asp291_Asp292del
ENST00000534358.5:c.4734_4739del	ENSP00000436786.1:p.Asp1579_Asp1580del
NM_001197104.1:c.4734_4739del , LRG_613t1:c.4734_4739del	NP_001184033.1:p.Asp1579_Asp1580del
NM_005933.3:c.4734_4739del	NP_005924.2:p.Asp1579_Asp1580del
XM_006718839.2:c.2217_2222del	XP_006718902.2:p.Asp740_Asp741del
XM_011542829.1:c.4833_4838del	XP_011541131.1:p.Asp1612_Asp1613del
XM_011542830.1:c.4830_4835del	XP_011541132.1:p.Asp1611_Asp1612del
XM_011542831.1:c.4833_4838del	XP_011541133.1:p.Asp1612_Asp1613del
XM_011542832.1:c.2640_2645del	XP_011541134.1:p.Asp881_Asp882del
XM_011542833.1:c.2316_2321del	XP_011541135.1:p.Asp773_Asp774del
XM_006718839.3:c.2217_2222del	XP_006718902.2:p.Asp740_Asp741del
XM_011542829.2:c.4833_4838del	XP_011541131.1:p.Asp1612_Asp1613del
XM_011542830.2:c.4830_4835del	XP_011541132.1:p.Asp1611_Asp1612del
XM_011542831.2:c.4833_4838del	XP_011541133.1:p.Asp1612_Asp1613del
XM_011542833.2:c.2316_2321del	XP_011541135.1:p.Asp773_Asp774del
NM_001197104.2:c.4734_4739del MANE Select	NP_001184033.1:p.Asp1579_Asp1580del
NM_005933.4:c.4734_4739del	NP_005924.2:p.Asp1579_Asp1580del