Canonical Allele Identifier: CA384682340

Gene: KMT2D

Linked Data

• ClinVar Variation Id: 463011
• ClinVar RCV Id: RCV000555530
• dbSNP Id: rs1555185299
• MyVariant Identifiers: chr12:g.49418592C>T (hg19) ; chr12:g.49024809C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.49024809C>T , CM000674.2:g.49024809C>T	GRCh38
NC_000012.11:g.49418592C>T , CM000674.1:g.49418592C>T	GRCh37
NC_000012.10:g.47704859C>T	NCBI36
NG_027827.1:g.35516G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000681974.1:n.593+1G>A
ENST00000683543.2:c.15921+1G>A	ENSP00000506726.1:n.15921+1G>A
ENST00000683863.1:n.1636+1G>A
ENST00000684428.1:c.456+1G>A	ENSP00000507433.1:n.456+1G>A
ENST00000684755.1:n.456+1G>A
ENST00000685024.1:c.1046+1G>A
ENST00000685166.1:c.15930+1G>A	ENSP00000509386.1:n.15930+1G>A
ENST00000688411.1:c.398+1G>A	ENSP00000510146.1:n.398+1G>A
ENST00000692637.1:c.15918+1G>A	ENSP00000509666.1:n.15918+1G>A
ENST00000301067.12:c.15921+1G>A MANE Select	ENSP00000301067.7:n.15921+1G>A
ENST00000301067.11:c.15921+1G>A	ENSP00000301067.7:n.15921+1G>A
NM_003482.3:c.15921+1G>A	NP_003473.3:n.15921+1G>A
XM_005269162.3:c.15921+1G>A	XP_005269219.1:n.15921+1G>A
XM_006719614.2:c.15930+1G>A	XP_006719677.1:n.15930+1G>A
XM_006719616.2:c.15918+1G>A	XP_006719679.1:n.15918+1G>A
XM_011538770.1:c.15930+1G>A	XP_011537072.1:n.15930+1G>A
XM_011538771.1:c.15927+1G>A	XP_011537073.1:n.15927+1G>A
XM_011538772.1:c.15921+1G>A	XP_011537074.1:n.15921+1G>A
XM_011538773.1:c.15918+1G>A	XP_011537075.1:n.15918+1G>A
XM_011538774.1:c.15909+1G>A	XP_011537076.1:n.15909+1G>A
XM_011538775.1:c.15864+1G>A	XP_011537077.1:n.15864+1G>A
XM_011538776.1:c.15837+1G>A	XP_011537078.1:n.15837+1G>A
XR_944740.1:n.17109+1G>A
XM_005269162.4:c.15921+1G>A	XP_005269219.1:n.15921+1G>A
XM_006719614.4:c.15930+1G>A	XP_006719677.1:n.15930+1G>A
XM_006719616.3:c.15918+1G>A	XP_006719679.1:n.15918+1G>A
XM_011538770.2:c.15930+1G>A	XP_011537072.1:n.15930+1G>A
XM_011538771.2:c.15927+1G>A	XP_011537073.1:n.15927+1G>A
XM_011538772.2:c.15921+1G>A	XP_011537074.1:n.15921+1G>A
XM_011538773.2:c.15918+1G>A	XP_011537075.1:n.15918+1G>A
XM_011538774.2:c.15909+1G>A	XP_011537076.1:n.15909+1G>A
XM_011538776.2:c.15837+1G>A	XP_011537078.1:n.15837+1G>A
XR_001748874.1:n.16098+1G>A
NM_003482.4:c.15921+1G>A MANE Select	NP_003473.3:n.15921+1G>A