Canonical Allele Identifier: CA384627116

Gene: KMT2D

Linked Data

• MyVariant Identifiers: chr12:g.49435976C>G (hg19) ; chr12:g.49042193C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.49042193C>G , CM000674.2:g.49042193C>G	GRCh38
NC_000012.11:g.49435976C>G , CM000674.1:g.49435976C>G	GRCh37
NC_000012.10:g.47722243C>G	NCBI36
NG_027827.1:g.18132G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650290.2:c.796G>C
ENST00000683543.2:c.6005G>C	ENSP00000506726.1:p.Ser2002Thr
ENST00000685166.1:c.6014G>C	ENSP00000509386.1:p.Ser2005Thr
ENST00000689060.1:c.117G>C
ENST00000689944.1:c.117G>C
ENST00000692637.1:c.6002G>C	ENSP00000509666.1:p.Ser2001Thr
ENST00000301067.12:c.6005G>C MANE Select	ENSP00000301067.7:p.Ser2002Thr
ENST00000301067.11:c.6005G>C	ENSP00000301067.7:p.Ser2002Thr
NM_003482.3:c.6005G>C	NP_003473.3:p.Ser2002Thr
XM_005269162.3:c.6005G>C	XP_005269219.1:p.Ser2002Thr
XM_006719614.2:c.6014G>C	XP_006719677.1:p.Ser2005Thr
XM_006719616.2:c.6002G>C	XP_006719679.1:p.Ser2001Thr
XM_011538770.1:c.6014G>C	XP_011537072.1:p.Ser2005Thr
XM_011538771.1:c.6011G>C	XP_011537073.1:p.Ser2004Thr
XM_011538772.1:c.6005G>C	XP_011537074.1:p.Ser2002Thr
XM_011538773.1:c.6002G>C	XP_011537075.1:p.Ser2001Thr
XM_011538774.1:c.5993G>C	XP_011537076.1:p.Ser1998Thr
XM_011538775.1:c.6014G>C	XP_011537077.1:p.Ser2005Thr
XM_011538776.1:c.6014G>C	XP_011537078.1:p.Ser2005Thr
XR_944740.1:n.8334G>C
XM_005269162.4:c.6005G>C	XP_005269219.1:p.Ser2002Thr
XM_006719614.4:c.6014G>C	XP_006719677.1:p.Ser2005Thr
XM_006719616.3:c.6002G>C	XP_006719679.1:p.Ser2001Thr
XM_011538770.2:c.6014G>C	XP_011537072.1:p.Ser2005Thr
XM_011538771.2:c.6011G>C	XP_011537073.1:p.Ser2004Thr
XM_011538772.2:c.6005G>C	XP_011537074.1:p.Ser2002Thr
XM_011538773.2:c.6002G>C	XP_011537075.1:p.Ser2001Thr
XM_011538774.2:c.5993G>C	XP_011537076.1:p.Ser1998Thr
XM_011538776.2:c.6014G>C	XP_011537078.1:p.Ser2005Thr
XR_001748874.1:n.7323G>C
NM_003482.4:c.6005G>C MANE Select	NP_003473.3:p.Ser2002Thr