Canonical Allele Identifier: CA382802893

Gene: KMT2A

Linked Data

• MyVariant Identifiers: chr11:g.118373349C>A (hg19) ; chr11:g.118502634C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118502634C>A , CM000673.2:g.118502634C>A	GRCh38
NC_000011.9:g.118373349C>A , CM000673.1:g.118373349C>A	GRCh37
NC_000011.8:g.117878559C>A	NCBI36
NG_027813.1:g.71145C>A , LRG_613:g.71145C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000531904.7:c.6841C>A	ENSP00000432391.3:p.His2281Asn
ENST00000710560.1:c.6832C>A	ENSP00000518343.1:p.His2278Asn
ENST00000649878.2:c.781C>A	ENSP00000497891.2:p.His261Asn
ENST00000685397.1:c.781C>A	ENSP00000509586.1:p.His261Asn
ENST00000686370.1:c.781C>A	ENSP00000509179.1:p.His261Asn
ENST00000689424.1:c.1039C>A	ENSP00000509852.1:p.His347Asn
ENST00000691053.1:c.6814C>A	ENSP00000509168.1:p.His2272Asn
ENST00000389506.10:c.6733C>A	ENSP00000374157.5:p.His2245Asn
ENST00000528278.2:n.6084C>A
ENST00000534358.8:c.6742C>A MANE Select	ENSP00000436786.2:p.His2248Asn
ENST00000649699.1:c.6619C>A	ENSP00000496927.1:p.His2207Asn
ENST00000389506.9:c.6733C>A	ENSP00000374157.5:p.His2245Asn
ENST00000528278.1:n.869C>A
ENST00000534358.5:c.6742C>A	ENSP00000436786.1:p.His2248Asn
NM_001197104.1:c.6742C>A , LRG_613t1:c.6742C>A	NP_001184033.1:p.His2248Asn
NM_005933.3:c.6733C>A	NP_005924.2:p.His2245Asn
XM_006718839.2:c.4225C>A	XP_006718902.2:p.His1409Asn
XM_011542829.1:c.6841C>A	XP_011541131.1:p.His2281Asn
XM_011542830.1:c.6838C>A	XP_011541132.1:p.His2280Asn
XM_011542831.1:c.6832C>A	XP_011541133.1:p.His2278Asn
XM_011542832.1:c.4648C>A	XP_011541134.1:p.His1550Asn
XM_011542833.1:c.4324C>A	XP_011541135.1:p.His1442Asn
XM_006718839.3:c.4225C>A	XP_006718902.2:p.His1409Asn
XM_011542829.2:c.6841C>A	XP_011541131.1:p.His2281Asn
XM_011542830.2:c.6838C>A	XP_011541132.1:p.His2280Asn
XM_011542831.2:c.6832C>A	XP_011541133.1:p.His2278Asn
XM_011542833.2:c.4324C>A	XP_011541135.1:p.His1442Asn
NM_001197104.2:c.6742C>A MANE Select	NP_001184033.1:p.His2248Asn
NM_005933.4:c.6733C>A	NP_005924.2:p.His2245Asn