Canonical Allele Identifier: CA384714315

Gene: KMT2D

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.49032815G>A , CM000674.2:g.49032815G>A	GRCh38
NC_000012.11:g.49426598G>A , CM000674.1:g.49426598G>A	GRCh37
NC_000012.10:g.47712865G>A	NCBI36
NG_027827.1:g.27510C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_003482.4:c.11890C>T MANE Select	NP_003473.3:p.Gln3964Ter
ENST00000301067.12:c.11890C>T MANE Select	ENSP00000301067.7:p.Gln3964Ter
NM_003482.3:c.11890C>T	NP_003473.3:p.Gln3964Ter
ENST00000301067.11:c.11890C>T	ENSP00000301067.7:p.Gln3964Ter
ENST00000683543.2:c.11890C>T	ENSP00000506726.1:p.Gln3964Ter
ENST00000685166.1:c.11899C>T	ENSP00000509386.1:p.Gln3967Ter
ENST00000685554.1:c.1450C>T	ENSP00000508640.1:p.Gln484Ter
ENST00000687201.1:c.3469C>T	ENSP00000510037.1:p.Gln1157Ter
ENST00000692637.1:c.11887C>T	ENSP00000509666.1:p.Gln3963Ter
ENST00000692841.1:c.3369C>T	ENSP00000508711.1:n.3369C>T
XM_005269162.3:c.11890C>T	XP_005269219.1:p.Gln3964Ter
XM_005269162.4:c.11890C>T	XP_005269219.1:p.Gln3964Ter
XM_006719614.2:c.11899C>T	XP_006719677.1:p.Gln3967Ter
XM_006719614.4:c.11899C>T	XP_006719677.1:p.Gln3967Ter
XM_006719616.2:c.11887C>T	XP_006719679.1:p.Gln3963Ter
XM_006719616.3:c.11887C>T	XP_006719679.1:p.Gln3963Ter
XM_011538770.1:c.11899C>T	XP_011537072.1:p.Gln3967Ter
XM_011538770.2:c.11899C>T	XP_011537072.1:p.Gln3967Ter
XM_011538771.1:c.11896C>T	XP_011537073.1:p.Gln3966Ter
XM_011538771.2:c.11896C>T	XP_011537073.1:p.Gln3966Ter
XM_011538772.1:c.11890C>T	XP_011537074.1:p.Gln3964Ter
XM_011538772.2:c.11890C>T	XP_011537074.1:p.Gln3964Ter
XM_011538773.1:c.11887C>T	XP_011537075.1:p.Gln3963Ter
XM_011538773.2:c.11887C>T	XP_011537075.1:p.Gln3963Ter
XM_011538774.1:c.11878C>T	XP_011537076.1:p.Gln3960Ter
XM_011538774.2:c.11878C>T	XP_011537076.1:p.Gln3960Ter
XM_011538775.1:c.11899C>T	XP_011537077.1:p.Gln3967Ter
XM_011538776.1:c.11806C>T	XP_011537078.1:p.Gln3936Ter
XM_011538776.2:c.11806C>T	XP_011537078.1:p.Gln3936Ter
XR_001748874.1:n.13208C>T
XR_944740.1:n.14219C>T