Canonical Allele Identifier: CA382805722

Gene: KMT2A

Linked Data

• MyVariant Identifiers: chr11:g.118374081G>A (hg19) ; chr11:g.118503366G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118503366G>A , CM000673.2:g.118503366G>A	GRCh38
NC_000011.9:g.118374081G>A , CM000673.1:g.118374081G>A	GRCh37
NC_000011.8:g.117879291G>A	NCBI36
NG_027813.1:g.71877G>A , LRG_613:g.71877G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000531904.7:c.7573G>A	ENSP00000432391.3:p.Asp2525Asn
ENST00000710560.1:c.7564G>A	ENSP00000518343.1:p.Asp2522Asn
ENST00000649878.2:c.1513G>A	ENSP00000497891.2:p.Asp505Asn
ENST00000685397.1:c.1513G>A	ENSP00000509586.1:p.Asp505Asn
ENST00000686370.1:c.1513G>A	ENSP00000509179.1:p.Asp505Asn
ENST00000689424.1:c.1771G>A	ENSP00000509852.1:p.Asp591Asn
ENST00000691053.1:c.7546G>A	ENSP00000509168.1:p.Asp2516Asn
ENST00000389506.10:c.7465G>A	ENSP00000374157.5:p.Asp2489Asn
ENST00000528278.2:n.6816G>A
ENST00000534358.8:c.7474G>A MANE Select	ENSP00000436786.2:p.Asp2492Asn
ENST00000649699.1:c.7351G>A	ENSP00000496927.1:p.Asp2451Asn
ENST00000389506.9:c.7465G>A	ENSP00000374157.5:p.Asp2489Asn
ENST00000528278.1:n.1601G>A
ENST00000534358.5:c.7474G>A	ENSP00000436786.1:p.Asp2492Asn
NM_001197104.1:c.7474G>A , LRG_613t1:c.7474G>A	NP_001184033.1:p.Asp2492Asn
NM_005933.3:c.7465G>A	NP_005924.2:p.Asp2489Asn
XM_006718839.2:c.4957G>A	XP_006718902.2:p.Asp1653Asn
XM_011542829.1:c.7573G>A	XP_011541131.1:p.Asp2525Asn
XM_011542830.1:c.7570G>A	XP_011541132.1:p.Asp2524Asn
XM_011542831.1:c.7564G>A	XP_011541133.1:p.Asp2522Asn
XM_011542832.1:c.5380G>A	XP_011541134.1:p.Asp1794Asn
XM_011542833.1:c.5056G>A	XP_011541135.1:p.Asp1686Asn
XM_006718839.3:c.4957G>A	XP_006718902.2:p.Asp1653Asn
XM_011542829.2:c.7573G>A	XP_011541131.1:p.Asp2525Asn
XM_011542830.2:c.7570G>A	XP_011541132.1:p.Asp2524Asn
XM_011542831.2:c.7564G>A	XP_011541133.1:p.Asp2522Asn
XM_011542833.2:c.5056G>A	XP_011541135.1:p.Asp1686Asn
NM_001197104.2:c.7474G>A MANE Select	NP_001184033.1:p.Asp2492Asn
NM_005933.4:c.7465G>A	NP_005924.2:p.Asp2489Asn