Canonical Allele Identifier: CA384649318

Gene: KMT2D

Linked Data

• MyVariant Identifiers: chr12:g.49441785C>A (hg19) ; chr12:g.49048002C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.49048002C>A , CM000674.2:g.49048002C>A	GRCh38
NC_000012.11:g.49441785C>A , CM000674.1:g.49441785C>A	GRCh37
NC_000012.10:g.47728052C>A	NCBI36
NG_027827.1:g.12323G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683543.2:c.4199G>T	ENSP00000506726.1:p.Cys1400Phe
ENST00000685166.1:c.4199G>T	ENSP00000509386.1:p.Cys1400Phe
ENST00000688095.1:c.179G>T	ENSP00000510007.1:p.Cys60Phe
ENST00000692637.1:c.4196G>T	ENSP00000509666.1:p.Cys1399Phe
ENST00000301067.12:c.4199G>T MANE Select	ENSP00000301067.7:p.Cys1400Phe
ENST00000301067.11:c.4199G>T	ENSP00000301067.7:p.Cys1400Phe
NM_003482.3:c.4199G>T	NP_003473.3:p.Cys1400Phe
XM_005269162.3:c.4199G>T	XP_005269219.1:p.Cys1400Phe
XM_006719614.2:c.4199G>T	XP_006719677.1:p.Cys1400Phe
XM_006719616.2:c.4196G>T	XP_006719679.1:p.Cys1399Phe
XM_011538770.1:c.4199G>T	XP_011537072.1:p.Cys1400Phe
XM_011538771.1:c.4196G>T	XP_011537073.1:p.Cys1399Phe
XM_011538772.1:c.4199G>T	XP_011537074.1:p.Cys1400Phe
XM_011538773.1:c.4196G>T	XP_011537075.1:p.Cys1399Phe
XM_011538774.1:c.4199G>T	XP_011537076.1:p.Cys1400Phe
XM_011538775.1:c.4199G>T	XP_011537077.1:p.Cys1400Phe
XM_011538776.1:c.4199G>T	XP_011537078.1:p.Cys1400Phe
XR_944740.1:n.6519G>T
XM_005269162.4:c.4199G>T	XP_005269219.1:p.Cys1400Phe
XM_006719614.4:c.4199G>T	XP_006719677.1:p.Cys1400Phe
XM_006719616.3:c.4196G>T	XP_006719679.1:p.Cys1399Phe
XM_011538770.2:c.4199G>T	XP_011537072.1:p.Cys1400Phe
XM_011538771.2:c.4196G>T	XP_011537073.1:p.Cys1399Phe
XM_011538772.2:c.4199G>T	XP_011537074.1:p.Cys1400Phe
XM_011538773.2:c.4196G>T	XP_011537075.1:p.Cys1399Phe
XM_011538774.2:c.4199G>T	XP_011537076.1:p.Cys1400Phe
XM_011538776.2:c.4199G>T	XP_011537078.1:p.Cys1400Phe
XR_001748874.1:n.5508G>T
NM_003482.4:c.4199G>T MANE Select	NP_003473.3:p.Cys1400Phe