Canonical Allele Identifier: CA477088738

Gene: KMT2A

Linked Data

• MyVariant Identifiers: chr11:g.118350931C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118480216C>G , CM000673.2:g.118480216C>G	GRCh38
NC_000011.9:g.118350931C>G , CM000673.1:g.118350931C>G	GRCh37
NC_000011.8:g.117856141C>G	NCBI36
NG_027813.1:g.48727C>G , LRG_613:g.48727C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000531904.7:c.3711C>G	ENSP00000432391.3:p.Ala1237=
ENST00000710560.1:c.3711C>G	ENSP00000518343.1:p.Ala1237=
ENST00000527869.7:c.1194C>G	ENSP00000432652.3:p.Ala398=
ENST00000533790.3:c.1095C>G	ENSP00000436700.3:p.Ala365=
ENST00000649690.2:c.1419C>G	ENSP00000497372.2:p.Ala473=
ENST00000685719.1:c.593C>G
ENST00000691053.1:c.3612C>G	ENSP00000509168.1:p.Ala1204=
ENST00000389506.10:c.3612C>G	ENSP00000374157.5:p.Ala1204=
ENST00000533790.2:c.864C>G	ENSP00000436700.2:p.Ala288=
ENST00000534358.8:c.3612C>G MANE Select	ENSP00000436786.2:p.Ala1204=
ENST00000648261.1:c.2382C>G	ENSP00000498126.1:p.Ala794=
ENST00000649699.1:c.3612C>G	ENSP00000496927.1:p.Ala1204=
ENST00000389506.9:c.3612C>G	ENSP00000374157.5:p.Ala1204=
ENST00000531904.6:c.3711C>G	ENSP00000432391.2:p.Ala1237=
ENST00000534358.5:c.3612C>G	ENSP00000436786.1:p.Ala1204=
NM_001197104.1:c.3612C>G , LRG_613t1:c.3612C>G	NP_001184033.1:p.Ala1204=
NM_005933.3:c.3612C>G	NP_005924.2:p.Ala1204=
XM_006718839.2:c.1095C>G	XP_006718902.2:p.Ala365=
XM_011542829.1:c.3711C>G	XP_011541131.1:p.Ala1237=
XM_011542830.1:c.3711C>G	XP_011541132.1:p.Ala1237=
XM_011542831.1:c.3711C>G	XP_011541133.1:p.Ala1237=
XM_011542832.1:c.1518C>G	XP_011541134.1:p.Ala506=
XM_011542833.1:c.1194C>G	XP_011541135.1:p.Ala398=
XM_006718839.3:c.1095C>G	XP_006718902.2:p.Ala365=
XM_011542829.2:c.3711C>G	XP_011541131.1:p.Ala1237=
XM_011542830.2:c.3711C>G	XP_011541132.1:p.Ala1237=
XM_011542831.2:c.3711C>G	XP_011541133.1:p.Ala1237=
XM_011542833.2:c.1194C>G	XP_011541135.1:p.Ala398=
NM_001197104.2:c.3612C>G MANE Select	NP_001184033.1:p.Ala1204=
NM_005933.4:c.3612C>G	NP_005924.2:p.Ala1204=