Canonical Allele Identifier: CA382805354

Gene: KMT2A

Linked Data

• MyVariant Identifiers: chr11:g.118373994T>G (hg19) ; chr11:g.118503279T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118503279T>G , CM000673.2:g.118503279T>G	GRCh38
NC_000011.9:g.118373994T>G , CM000673.1:g.118373994T>G	GRCh37
NC_000011.8:g.117879204T>G	NCBI36
NG_027813.1:g.71790T>G , LRG_613:g.71790T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000531904.7:c.7486T>G	ENSP00000432391.3:p.Leu2496Val
ENST00000710560.1:c.7477T>G	ENSP00000518343.1:p.Leu2493Val
ENST00000649878.2:c.1426T>G	ENSP00000497891.2:p.Leu476Val
ENST00000685397.1:c.1426T>G	ENSP00000509586.1:p.Leu476Val
ENST00000686370.1:c.1426T>G	ENSP00000509179.1:p.Leu476Val
ENST00000689424.1:c.1684T>G	ENSP00000509852.1:p.Leu562Val
ENST00000691053.1:c.7459T>G	ENSP00000509168.1:p.Leu2487Val
ENST00000389506.10:c.7378T>G	ENSP00000374157.5:p.Leu2460Val
ENST00000528278.2:n.6729T>G
ENST00000534358.8:c.7387T>G MANE Select	ENSP00000436786.2:p.Leu2463Val
ENST00000649699.1:c.7264T>G	ENSP00000496927.1:p.Leu2422Val
ENST00000389506.9:c.7378T>G	ENSP00000374157.5:p.Leu2460Val
ENST00000528278.1:n.1514T>G
ENST00000534358.5:c.7387T>G	ENSP00000436786.1:p.Leu2463Val
NM_001197104.1:c.7387T>G , LRG_613t1:c.7387T>G	NP_001184033.1:p.Leu2463Val
NM_005933.3:c.7378T>G	NP_005924.2:p.Leu2460Val
XM_006718839.2:c.4870T>G	XP_006718902.2:p.Leu1624Val
XM_011542829.1:c.7486T>G	XP_011541131.1:p.Leu2496Val
XM_011542830.1:c.7483T>G	XP_011541132.1:p.Leu2495Val
XM_011542831.1:c.7477T>G	XP_011541133.1:p.Leu2493Val
XM_011542832.1:c.5293T>G	XP_011541134.1:p.Leu1765Val
XM_011542833.1:c.4969T>G	XP_011541135.1:p.Leu1657Val
XM_006718839.3:c.4870T>G	XP_006718902.2:p.Leu1624Val
XM_011542829.2:c.7486T>G	XP_011541131.1:p.Leu2496Val
XM_011542830.2:c.7483T>G	XP_011541132.1:p.Leu2495Val
XM_011542831.2:c.7477T>G	XP_011541133.1:p.Leu2493Val
XM_011542833.2:c.4969T>G	XP_011541135.1:p.Leu1657Val
NM_001197104.2:c.7387T>G MANE Select	NP_001184033.1:p.Leu2463Val
NM_005933.4:c.7378T>G	NP_005924.2:p.Leu2460Val