Canonical Allele Identifier: CA384688562

Gene: KMT2D

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.49026617A>C , CM000674.2:g.49026617A>C	GRCh38
NC_000012.11:g.49420400A>C , CM000674.1:g.49420400A>C	GRCh37
NC_000012.10:g.47706667A>C	NCBI36
NG_027827.1:g.33708T>G

Transcript Alleles

HGVS	Amino-acid Change
NM_003482.4:c.15349T>G MANE Select	NP_003473.3:p.Cys5117Gly
ENST00000301067.12:c.15349T>G MANE Select	ENSP00000301067.7:p.Cys5117Gly
NM_003482.3:c.15349T>G	NP_003473.3:p.Cys5117Gly
ENST00000301067.11:c.15349T>G	ENSP00000301067.7:p.Cys5117Gly
ENST00000683543.2:c.15349T>G	ENSP00000506726.1:p.Cys5117Gly
ENST00000685024.1:c.474T>G
ENST00000685166.1:c.15358T>G	ENSP00000509386.1:p.Cys5120Gly
ENST00000688411.1:c.261+1186T>G	ENSP00000510146.1:n.261+1186T>G
ENST00000691463.1:c.735T>G	ENSP00000510624.1:n.735T>G
ENST00000692637.1:c.15346T>G	ENSP00000509666.1:p.Cys5116Gly
XM_005269162.3:c.15349T>G	XP_005269219.1:p.Cys5117Gly
XM_005269162.4:c.15349T>G	XP_005269219.1:p.Cys5117Gly
XM_006719614.2:c.15358T>G	XP_006719677.1:p.Cys5120Gly
XM_006719614.4:c.15358T>G	XP_006719677.1:p.Cys5120Gly
XM_006719616.2:c.15346T>G	XP_006719679.1:p.Cys5116Gly
XM_006719616.3:c.15346T>G	XP_006719679.1:p.Cys5116Gly
XM_011538770.1:c.15358T>G	XP_011537072.1:p.Cys5120Gly
XM_011538770.2:c.15358T>G	XP_011537072.1:p.Cys5120Gly
XM_011538771.1:c.15355T>G	XP_011537073.1:p.Cys5119Gly
XM_011538771.2:c.15355T>G	XP_011537073.1:p.Cys5119Gly
XM_011538772.1:c.15349T>G	XP_011537074.1:p.Cys5117Gly
XM_011538772.2:c.15349T>G	XP_011537074.1:p.Cys5117Gly
XM_011538773.1:c.15346T>G	XP_011537075.1:p.Cys5116Gly
XM_011538773.2:c.15346T>G	XP_011537075.1:p.Cys5116Gly
XM_011538774.1:c.15337T>G	XP_011537076.1:p.Cys5113Gly
XM_011538774.2:c.15337T>G	XP_011537076.1:p.Cys5113Gly
XM_011538775.1:c.15292T>G	XP_011537077.1:p.Cys5098Gly
XM_011538776.1:c.15265T>G	XP_011537078.1:p.Cys5089Gly
XM_011538776.2:c.15265T>G	XP_011537078.1:p.Cys5089Gly
XR_001748874.1:n.15961+1186T>G
XR_944740.1:n.16972+1186T>G