Canonical Allele Identifier: CA384682406

Gene: KMT2D

Linked Data

• dbSNP Id: rs2137711358
• gnomAD v4: 12-49024817-G-A
• MyVariant Identifiers: chr12:g.49418600G>A (hg19) ; chr12:g.49024817G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.49024817G>A , CM000674.2:g.49024817G>A	GRCh38
NC_000012.11:g.49418600G>A , CM000674.1:g.49418600G>A	GRCh37
NC_000012.10:g.47704867G>A	NCBI36
NG_027827.1:g.35508C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000681974.1:n.586C>T
ENST00000683543.2:c.15914C>T	ENSP00000506726.1:p.Ala5305Val
ENST00000683863.1:n.1629C>T
ENST00000684428.1:c.449C>T	ENSP00000507433.1:p.Ala150Val
ENST00000684755.1:n.449C>T
ENST00000685024.1:c.1039C>T
ENST00000685166.1:c.15923C>T	ENSP00000509386.1:p.Ala5308Val
ENST00000688411.1:c.391C>T	ENSP00000510146.1:n.391C>T
ENST00000691463.1:c.1300C>T	ENSP00000510624.1:n.1300C>T
ENST00000692637.1:c.15911C>T	ENSP00000509666.1:p.Ala5304Val
ENST00000301067.12:c.15914C>T MANE Select	ENSP00000301067.7:p.Ala5305Val
ENST00000301067.11:c.15914C>T	ENSP00000301067.7:p.Ala5305Val
NM_003482.3:c.15914C>T	NP_003473.3:p.Ala5305Val
XM_005269162.3:c.15914C>T	XP_005269219.1:p.Ala5305Val
XM_006719614.2:c.15923C>T	XP_006719677.1:p.Ala5308Val
XM_006719616.2:c.15911C>T	XP_006719679.1:p.Ala5304Val
XM_011538770.1:c.15923C>T	XP_011537072.1:p.Ala5308Val
XM_011538771.1:c.15920C>T	XP_011537073.1:p.Ala5307Val
XM_011538772.1:c.15914C>T	XP_011537074.1:p.Ala5305Val
XM_011538773.1:c.15911C>T	XP_011537075.1:p.Ala5304Val
XM_011538774.1:c.15902C>T	XP_011537076.1:p.Ala5301Val
XM_011538775.1:c.15857C>T	XP_011537077.1:p.Ala5286Val
XM_011538776.1:c.15830C>T	XP_011537078.1:p.Ala5277Val
XR_944740.1:n.17102C>T
XM_005269162.4:c.15914C>T	XP_005269219.1:p.Ala5305Val
XM_006719614.4:c.15923C>T	XP_006719677.1:p.Ala5308Val
XM_006719616.3:c.15911C>T	XP_006719679.1:p.Ala5304Val
XM_011538770.2:c.15923C>T	XP_011537072.1:p.Ala5308Val
XM_011538771.2:c.15920C>T	XP_011537073.1:p.Ala5307Val
XM_011538772.2:c.15914C>T	XP_011537074.1:p.Ala5305Val
XM_011538773.2:c.15911C>T	XP_011537075.1:p.Ala5304Val
XM_011538774.2:c.15902C>T	XP_011537076.1:p.Ala5301Val
XM_011538776.2:c.15830C>T	XP_011537078.1:p.Ala5277Val
XR_001748874.1:n.16091C>T
NM_003482.4:c.15914C>T MANE Select	NP_003473.3:p.Ala5305Val