Canonical Allele Identifier: CA382802634

Gene: KMT2A

Linked Data

• MyVariant Identifiers: chr11:g.118373280A>G (hg19) ; chr11:g.118502565A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118502565A>G , CM000673.2:g.118502565A>G	GRCh38
NC_000011.9:g.118373280A>G , CM000673.1:g.118373280A>G	GRCh37
NC_000011.8:g.117878490A>G	NCBI36
NG_027813.1:g.71076A>G , LRG_613:g.71076A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000531904.7:c.6772A>G	ENSP00000432391.3:p.Asn2258Asp
ENST00000710560.1:c.6763A>G	ENSP00000518343.1:p.Asn2255Asp
ENST00000649878.2:c.712A>G	ENSP00000497891.2:p.Asn238Asp
ENST00000685397.1:c.712A>G	ENSP00000509586.1:p.Asn238Asp
ENST00000686370.1:c.712A>G	ENSP00000509179.1:p.Asn238Asp
ENST00000689424.1:c.970A>G	ENSP00000509852.1:p.Asn324Asp
ENST00000691053.1:c.6745A>G	ENSP00000509168.1:p.Asn2249Asp
ENST00000389506.10:c.6664A>G	ENSP00000374157.5:p.Asn2222Asp
ENST00000528278.2:n.6015A>G
ENST00000534358.8:c.6673A>G MANE Select	ENSP00000436786.2:p.Asn2225Asp
ENST00000649699.1:c.6550A>G	ENSP00000496927.1:p.Asn2184Asp
ENST00000389506.9:c.6664A>G	ENSP00000374157.5:p.Asn2222Asp
ENST00000528278.1:n.800A>G
ENST00000534358.5:c.6673A>G	ENSP00000436786.1:p.Asn2225Asp
NM_001197104.1:c.6673A>G , LRG_613t1:c.6673A>G	NP_001184033.1:p.Asn2225Asp
NM_005933.3:c.6664A>G	NP_005924.2:p.Asn2222Asp
XM_006718839.2:c.4156A>G	XP_006718902.2:p.Asn1386Asp
XM_011542829.1:c.6772A>G	XP_011541131.1:p.Asn2258Asp
XM_011542830.1:c.6769A>G	XP_011541132.1:p.Asn2257Asp
XM_011542831.1:c.6763A>G	XP_011541133.1:p.Asn2255Asp
XM_011542832.1:c.4579A>G	XP_011541134.1:p.Asn1527Asp
XM_011542833.1:c.4255A>G	XP_011541135.1:p.Asn1419Asp
XM_006718839.3:c.4156A>G	XP_006718902.2:p.Asn1386Asp
XM_011542829.2:c.6772A>G	XP_011541131.1:p.Asn2258Asp
XM_011542830.2:c.6769A>G	XP_011541132.1:p.Asn2257Asp
XM_011542831.2:c.6763A>G	XP_011541133.1:p.Asn2255Asp
XM_011542833.2:c.4255A>G	XP_011541135.1:p.Asn1419Asp
NM_001197104.2:c.6673A>G MANE Select	NP_001184033.1:p.Asn2225Asp
NM_005933.4:c.6664A>G	NP_005924.2:p.Asn2222Asp