Canonical Allele Identifier: CA382805205

Gene: KMT2A

Linked Data

• MyVariant Identifiers: chr11:g.118373953T>G (hg19) ; chr11:g.118503238T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118503238T>G , CM000673.2:g.118503238T>G	GRCh38
NC_000011.9:g.118373953T>G , CM000673.1:g.118373953T>G	GRCh37
NC_000011.8:g.117879163T>G	NCBI36
NG_027813.1:g.71749T>G , LRG_613:g.71749T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000531904.7:c.7445T>G	ENSP00000432391.3:p.Phe2482Cys
ENST00000710560.1:c.7436T>G	ENSP00000518343.1:p.Phe2479Cys
ENST00000649878.2:c.1385T>G	ENSP00000497891.2:p.Phe462Cys
ENST00000685397.1:c.1385T>G	ENSP00000509586.1:p.Phe462Cys
ENST00000686370.1:c.1385T>G	ENSP00000509179.1:p.Phe462Cys
ENST00000689424.1:c.1643T>G	ENSP00000509852.1:p.Phe548Cys
ENST00000691053.1:c.7418T>G	ENSP00000509168.1:p.Phe2473Cys
ENST00000389506.10:c.7337T>G	ENSP00000374157.5:p.Phe2446Cys
ENST00000528278.2:n.6688T>G
ENST00000534358.8:c.7346T>G MANE Select	ENSP00000436786.2:p.Phe2449Cys
ENST00000649699.1:c.7223T>G	ENSP00000496927.1:p.Phe2408Cys
ENST00000389506.9:c.7337T>G	ENSP00000374157.5:p.Phe2446Cys
ENST00000528278.1:n.1473T>G
ENST00000534358.5:c.7346T>G	ENSP00000436786.1:p.Phe2449Cys
NM_001197104.1:c.7346T>G , LRG_613t1:c.7346T>G	NP_001184033.1:p.Phe2449Cys
NM_005933.3:c.7337T>G	NP_005924.2:p.Phe2446Cys
XM_006718839.2:c.4829T>G	XP_006718902.2:p.Phe1610Cys
XM_011542829.1:c.7445T>G	XP_011541131.1:p.Phe2482Cys
XM_011542830.1:c.7442T>G	XP_011541132.1:p.Phe2481Cys
XM_011542831.1:c.7436T>G	XP_011541133.1:p.Phe2479Cys
XM_011542832.1:c.5252T>G	XP_011541134.1:p.Phe1751Cys
XM_011542833.1:c.4928T>G	XP_011541135.1:p.Phe1643Cys
XM_006718839.3:c.4829T>G	XP_006718902.2:p.Phe1610Cys
XM_011542829.2:c.7445T>G	XP_011541131.1:p.Phe2482Cys
XM_011542830.2:c.7442T>G	XP_011541132.1:p.Phe2481Cys
XM_011542831.2:c.7436T>G	XP_011541133.1:p.Phe2479Cys
XM_011542833.2:c.4928T>G	XP_011541135.1:p.Phe1643Cys
NM_001197104.2:c.7346T>G MANE Select	NP_001184033.1:p.Phe2449Cys
NM_005933.4:c.7337T>G	NP_005924.2:p.Phe2446Cys