Canonical Allele Identifier: CA382805573

Gene: KMT2A

Linked Data

• MyVariant Identifiers: chr11:g.118374043A>G (hg19) ; chr11:g.118503328A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118503328A>G , CM000673.2:g.118503328A>G	GRCh38
NC_000011.9:g.118374043A>G , CM000673.1:g.118374043A>G	GRCh37
NC_000011.8:g.117879253A>G	NCBI36
NG_027813.1:g.71839A>G , LRG_613:g.71839A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000531904.7:c.7535A>G	ENSP00000432391.3:p.Gln2512Arg
ENST00000710560.1:c.7526A>G	ENSP00000518343.1:p.Gln2509Arg
ENST00000649878.2:c.1475A>G	ENSP00000497891.2:p.Gln492Arg
ENST00000685397.1:c.1475A>G	ENSP00000509586.1:p.Gln492Arg
ENST00000686370.1:c.1475A>G	ENSP00000509179.1:p.Gln492Arg
ENST00000689424.1:c.1733A>G	ENSP00000509852.1:p.Gln578Arg
ENST00000691053.1:c.7508A>G	ENSP00000509168.1:p.Gln2503Arg
ENST00000389506.10:c.7427A>G	ENSP00000374157.5:p.Gln2476Arg
ENST00000528278.2:n.6778A>G
ENST00000534358.8:c.7436A>G MANE Select	ENSP00000436786.2:p.Gln2479Arg
ENST00000649699.1:c.7313A>G	ENSP00000496927.1:p.Gln2438Arg
ENST00000389506.9:c.7427A>G	ENSP00000374157.5:p.Gln2476Arg
ENST00000528278.1:n.1563A>G
ENST00000534358.5:c.7436A>G	ENSP00000436786.1:p.Gln2479Arg
NM_001197104.1:c.7436A>G , LRG_613t1:c.7436A>G	NP_001184033.1:p.Gln2479Arg
NM_005933.3:c.7427A>G	NP_005924.2:p.Gln2476Arg
XM_006718839.2:c.4919A>G	XP_006718902.2:p.Gln1640Arg
XM_011542829.1:c.7535A>G	XP_011541131.1:p.Gln2512Arg
XM_011542830.1:c.7532A>G	XP_011541132.1:p.Gln2511Arg
XM_011542831.1:c.7526A>G	XP_011541133.1:p.Gln2509Arg
XM_011542832.1:c.5342A>G	XP_011541134.1:p.Gln1781Arg
XM_011542833.1:c.5018A>G	XP_011541135.1:p.Gln1673Arg
XM_006718839.3:c.4919A>G	XP_006718902.2:p.Gln1640Arg
XM_011542829.2:c.7535A>G	XP_011541131.1:p.Gln2512Arg
XM_011542830.2:c.7532A>G	XP_011541132.1:p.Gln2511Arg
XM_011542831.2:c.7526A>G	XP_011541133.1:p.Gln2509Arg
XM_011542833.2:c.5018A>G	XP_011541135.1:p.Gln1673Arg
NM_001197104.2:c.7436A>G MANE Select	NP_001184033.1:p.Gln2479Arg
NM_005933.4:c.7427A>G	NP_005924.2:p.Gln2476Arg