Canonical Allele Identifier: CA477359328

Gene: KMT2A

Linked Data

• MyVariant Identifiers: chr11:g.118373942C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118503227C>A , CM000673.2:g.118503227C>A	GRCh38
NC_000011.9:g.118373942C>A , CM000673.1:g.118373942C>A	GRCh37
NC_000011.8:g.117879152C>A	NCBI36
NG_027813.1:g.71738C>A , LRG_613:g.71738C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000531904.7:c.7434C>A	ENSP00000432391.3:p.Ser2478=
ENST00000710560.1:c.7425C>A	ENSP00000518343.1:p.Ser2475=
ENST00000649878.2:c.1374C>A	ENSP00000497891.2:p.Ser458=
ENST00000685397.1:c.1374C>A	ENSP00000509586.1:p.Ser458=
ENST00000686370.1:c.1374C>A	ENSP00000509179.1:p.Ser458=
ENST00000689424.1:c.1632C>A	ENSP00000509852.1:p.Ser544=
ENST00000691053.1:c.7407C>A	ENSP00000509168.1:p.Ser2469=
ENST00000389506.10:c.7326C>A	ENSP00000374157.5:p.Ser2442=
ENST00000528278.2:n.6677C>A
ENST00000534358.8:c.7335C>A MANE Select	ENSP00000436786.2:p.Ser2445=
ENST00000649699.1:c.7212C>A	ENSP00000496927.1:p.Ser2404=
ENST00000389506.9:c.7326C>A	ENSP00000374157.5:p.Ser2442=
ENST00000528278.1:n.1462C>A
ENST00000534358.5:c.7335C>A	ENSP00000436786.1:p.Ser2445=
NM_001197104.1:c.7335C>A , LRG_613t1:c.7335C>A	NP_001184033.1:p.Ser2445=
NM_005933.3:c.7326C>A	NP_005924.2:p.Ser2442=
XM_006718839.2:c.4818C>A	XP_006718902.2:p.Ser1606=
XM_011542829.1:c.7434C>A	XP_011541131.1:p.Ser2478=
XM_011542830.1:c.7431C>A	XP_011541132.1:p.Ser2477=
XM_011542831.1:c.7425C>A	XP_011541133.1:p.Ser2475=
XM_011542832.1:c.5241C>A	XP_011541134.1:p.Ser1747=
XM_011542833.1:c.4917C>A	XP_011541135.1:p.Ser1639=
XM_006718839.3:c.4818C>A	XP_006718902.2:p.Ser1606=
XM_011542829.2:c.7434C>A	XP_011541131.1:p.Ser2478=
XM_011542830.2:c.7431C>A	XP_011541132.1:p.Ser2477=
XM_011542831.2:c.7425C>A	XP_011541133.1:p.Ser2475=
XM_011542833.2:c.4917C>A	XP_011541135.1:p.Ser1639=
NM_001197104.2:c.7335C>A MANE Select	NP_001184033.1:p.Ser2445=
NM_005933.4:c.7326C>A	NP_005924.2:p.Ser2442=