Canonical Allele Identifier: CA382831625

Gene: KMT2A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118488612A>G , CM000673.2:g.118488612A>G	GRCh38
NC_000011.9:g.118359327A>G , CM000673.1:g.118359327A>G	GRCh37
NC_000011.8:g.117864537A>G	NCBI36
NG_027813.1:g.57123A>G , LRG_613:g.57123A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001197104.2:c.4333-2A>G MANE Select	NP_001184033.1:n.4333-2A>G
ENST00000534358.8:c.4333-2A>G MANE Select	ENSP00000436786.2:n.4333-2A>G
NM_001197104.1:c.4333-2A>G , LRG_613t1:c.4333-2A>G	NP_001184033.1:n.4333-2A>G
NM_005933.3:c.4333-2A>G	NP_005924.2:n.4333-2A>G
NM_005933.4:c.4333-2A>G	NP_005924.2:n.4333-2A>G
ENST00000389506.10:c.4333-2A>G	ENSP00000374157.5:n.4333-2A>G
ENST00000389506.9:c.4333-2A>G	ENSP00000374157.5:n.4333-2A>G
ENST00000392873.3:c.469-2A>G	ENSP00000376612.3:n.469-2A>G
ENST00000420751.4:c.244-2A>G	ENSP00000510776.1:n.244-2A>G
ENST00000531904.7:c.4432-2A>G	ENSP00000432391.3:n.4432-2A>G
ENST00000534358.5:c.4333-2A>G	ENSP00000436786.1:n.4333-2A>G
ENST00000649699.1:c.4219-2A>G	ENSP00000496927.1:n.4219-2A>G
ENST00000685498.1:c.112-2A>G	ENSP00000509293.1:n.112-2A>G
ENST00000691053.1:c.4333-2A>G	ENSP00000509168.1:n.4333-2A>G
ENST00000710560.1:c.4432-2A>G	ENSP00000518343.1:n.4432-2A>G
XM_006718839.2:c.1816-2A>G	XP_006718902.2:n.1816-2A>G
XM_006718839.3:c.1816-2A>G	XP_006718902.2:n.1816-2A>G
XM_011542829.1:c.4432-2A>G	XP_011541131.1:n.4432-2A>G
XM_011542829.2:c.4432-2A>G	XP_011541131.1:n.4432-2A>G
XM_011542830.1:c.4432-2A>G	XP_011541132.1:n.4432-2A>G
XM_011542830.2:c.4432-2A>G	XP_011541132.1:n.4432-2A>G
XM_011542831.1:c.4432-2A>G	XP_011541133.1:n.4432-2A>G
XM_011542831.2:c.4432-2A>G	XP_011541133.1:n.4432-2A>G
XM_011542832.1:c.2239-2A>G	XP_011541134.1:n.2239-2A>G
XM_011542833.1:c.1915-2A>G	XP_011541135.1:n.1915-2A>G
XM_011542833.2:c.1915-2A>G	XP_011541135.1:n.1915-2A>G