Canonical Allele Identifier: CA147659

Gene: KMT2D

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.49033869C>T , CM000674.2:g.49033869C>T	GRCh38
NC_000012.11:g.49427652C>T , CM000674.1:g.49427652C>T	GRCh37
NC_000012.10:g.47713919C>T	NCBI36
NG_027827.1:g.26456G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683543.2:c.10836G>A	ENSP00000506726.1:p.Gln3612=
ENST00000685166.1:c.10845G>A	ENSP00000509386.1:p.Gln3615=
ENST00000685554.1:c.396G>A	ENSP00000508640.1:p.Gln132=
ENST00000687201.1:c.2415G>A	ENSP00000510037.1:p.Gln805=
ENST00000692637.1:c.10833G>A	ENSP00000509666.1:p.Gln3611=
ENST00000692841.1:c.2315G>A	ENSP00000508711.1:n.2315G>A
ENST00000301067.12:c.10836G>A MANE Select	ENSP00000301067.7:p.Gln3612=
ENST00000301067.11:c.10836G>A	ENSP00000301067.7:p.Gln3612=
NM_003482.3:c.10836G>A	NP_003473.3:p.Gln3612=
XM_005269162.3:c.10836G>A	XP_005269219.1:p.Gln3612=
XM_006719614.2:c.10845G>A	XP_006719677.1:p.Gln3615=
XM_006719616.2:c.10833G>A	XP_006719679.1:p.Gln3611=
XM_011538770.1:c.10845G>A	XP_011537072.1:p.Gln3615=
XM_011538771.1:c.10842G>A	XP_011537073.1:p.Gln3614=
XM_011538772.1:c.10836G>A	XP_011537074.1:p.Gln3612=
XM_011538773.1:c.10833G>A	XP_011537075.1:p.Gln3611=
XM_011538774.1:c.10824G>A	XP_011537076.1:p.Gln3608=
XM_011538775.1:c.10845G>A	XP_011537077.1:p.Gln3615=
XM_011538776.1:c.10752G>A	XP_011537078.1:p.Gln3584=
XR_944740.1:n.13165G>A
XM_005269162.4:c.10836G>A	XP_005269219.1:p.Gln3612=
XM_006719614.4:c.10845G>A	XP_006719677.1:p.Gln3615=
XM_006719616.3:c.10833G>A	XP_006719679.1:p.Gln3611=
XM_011538770.2:c.10845G>A	XP_011537072.1:p.Gln3615=
XM_011538771.2:c.10842G>A	XP_011537073.1:p.Gln3614=
XM_011538772.2:c.10836G>A	XP_011537074.1:p.Gln3612=
XM_011538773.2:c.10833G>A	XP_011537075.1:p.Gln3611=
XM_011538774.2:c.10824G>A	XP_011537076.1:p.Gln3608=
XM_011538776.2:c.10752G>A	XP_011537078.1:p.Gln3584=
XR_001748874.1:n.12154G>A
NM_003482.4:c.10836G>A MANE Select	NP_003473.3:p.Gln3612=