Canonical Allele Identifier: CA384683160

Gene: KMT2D

Linked Data

• dbSNP Id: rs2137711785
• MyVariant Identifiers: chr12:g.49418666A>T (hg19) ; chr12:g.49024883A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.49024883A>T , CM000674.2:g.49024883A>T	GRCh38
NC_000012.11:g.49418666A>T , CM000674.1:g.49418666A>T	GRCh37
NC_000012.10:g.47704933A>T	NCBI36
NG_027827.1:g.35442T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000681974.1:n.520T>A
ENST00000683543.2:c.15848T>A	ENSP00000506726.1:p.Leu5283His
ENST00000683863.1:n.1563T>A
ENST00000684428.1:c.383T>A	ENSP00000507433.1:p.Leu128His
ENST00000684755.1:n.383T>A
ENST00000685024.1:c.973T>A
ENST00000685166.1:c.15857T>A	ENSP00000509386.1:p.Leu5286His
ENST00000688411.1:c.325T>A	ENSP00000510146.1:n.325T>A
ENST00000691463.1:c.1234T>A	ENSP00000510624.1:n.1234T>A
ENST00000692637.1:c.15845T>A	ENSP00000509666.1:p.Leu5282His
ENST00000301067.12:c.15848T>A MANE Select	ENSP00000301067.7:p.Leu5283His
ENST00000301067.11:c.15848T>A	ENSP00000301067.7:p.Leu5283His
NM_003482.3:c.15848T>A	NP_003473.3:p.Leu5283His
XM_005269162.3:c.15848T>A	XP_005269219.1:p.Leu5283His
XM_006719614.2:c.15857T>A	XP_006719677.1:p.Leu5286His
XM_006719616.2:c.15845T>A	XP_006719679.1:p.Leu5282His
XM_011538770.1:c.15857T>A	XP_011537072.1:p.Leu5286His
XM_011538771.1:c.15854T>A	XP_011537073.1:p.Leu5285His
XM_011538772.1:c.15848T>A	XP_011537074.1:p.Leu5283His
XM_011538773.1:c.15845T>A	XP_011537075.1:p.Leu5282His
XM_011538774.1:c.15836T>A	XP_011537076.1:p.Leu5279His
XM_011538775.1:c.15791T>A	XP_011537077.1:p.Leu5264His
XM_011538776.1:c.15764T>A	XP_011537078.1:p.Leu5255His
XR_944740.1:n.17036T>A
XM_005269162.4:c.15848T>A	XP_005269219.1:p.Leu5283His
XM_006719614.4:c.15857T>A	XP_006719677.1:p.Leu5286His
XM_006719616.3:c.15845T>A	XP_006719679.1:p.Leu5282His
XM_011538770.2:c.15857T>A	XP_011537072.1:p.Leu5286His
XM_011538771.2:c.15854T>A	XP_011537073.1:p.Leu5285His
XM_011538772.2:c.15848T>A	XP_011537074.1:p.Leu5283His
XM_011538773.2:c.15845T>A	XP_011537075.1:p.Leu5282His
XM_011538774.2:c.15836T>A	XP_011537076.1:p.Leu5279His
XM_011538776.2:c.15764T>A	XP_011537078.1:p.Leu5255His
XR_001748874.1:n.16025T>A
NM_003482.4:c.15848T>A MANE Select	NP_003473.3:p.Leu5283His