Canonical Allele Identifier: CA384747265

Gene: KMT2D

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.49040116G>T , CM000674.2:g.49040116G>T	GRCh38
NC_000012.11:g.49433899G>T , CM000674.1:g.49433899G>T	GRCh37
NC_000012.10:g.47720166G>T	NCBI36
NG_027827.1:g.20209C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_003482.4:c.7654C>A MANE Select	NP_003473.3:p.Pro2552Thr
ENST00000301067.12:c.7654C>A MANE Select	ENSP00000301067.7:p.Pro2552Thr
NM_003482.3:c.7654C>A	NP_003473.3:p.Pro2552Thr
ENST00000301067.11:c.7654C>A	ENSP00000301067.7:p.Pro2552Thr
ENST00000683543.2:c.7654C>A	ENSP00000506726.1:p.Pro2552Thr
ENST00000685166.1:c.7663C>A	ENSP00000509386.1:p.Pro2555Thr
ENST00000689060.1:c.1673C>A
ENST00000689143.1:c.1327C>A	ENSP00000509839.1:p.Pro443Thr
ENST00000689944.1:c.1763C>A
ENST00000692637.1:c.7651C>A	ENSP00000509666.1:p.Pro2551Thr
XM_005269162.3:c.7654C>A	XP_005269219.1:p.Pro2552Thr
XM_005269162.4:c.7654C>A	XP_005269219.1:p.Pro2552Thr
XM_006719614.2:c.7663C>A	XP_006719677.1:p.Pro2555Thr
XM_006719614.4:c.7663C>A	XP_006719677.1:p.Pro2555Thr
XM_006719616.2:c.7651C>A	XP_006719679.1:p.Pro2551Thr
XM_006719616.3:c.7651C>A	XP_006719679.1:p.Pro2551Thr
XM_011538770.1:c.7663C>A	XP_011537072.1:p.Pro2555Thr
XM_011538770.2:c.7663C>A	XP_011537072.1:p.Pro2555Thr
XM_011538771.1:c.7660C>A	XP_011537073.1:p.Pro2554Thr
XM_011538771.2:c.7660C>A	XP_011537073.1:p.Pro2554Thr
XM_011538772.1:c.7654C>A	XP_011537074.1:p.Pro2552Thr
XM_011538772.2:c.7654C>A	XP_011537074.1:p.Pro2552Thr
XM_011538773.1:c.7651C>A	XP_011537075.1:p.Pro2551Thr
XM_011538773.2:c.7651C>A	XP_011537075.1:p.Pro2551Thr
XM_011538774.1:c.7642C>A	XP_011537076.1:p.Pro2548Thr
XM_011538774.2:c.7642C>A	XP_011537076.1:p.Pro2548Thr
XM_011538775.1:c.7663C>A	XP_011537077.1:p.Pro2555Thr
XM_011538776.1:c.7570C>A	XP_011537078.1:p.Pro2524Thr
XM_011538776.2:c.7570C>A	XP_011537078.1:p.Pro2524Thr
XR_001748874.1:n.8972C>A
XR_944740.1:n.9983C>A