Canonical Allele Identifier: CA479712441

Gene: KMT2D

Linked Data

• MyVariant Identifiers: chr12:g.49435996T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.49042213T>G , CM000674.2:g.49042213T>G	GRCh38
NC_000012.11:g.49435996T>G , CM000674.1:g.49435996T>G	GRCh37
NC_000012.10:g.47722263T>G	NCBI36
NG_027827.1:g.18112A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650290.2:c.776A>C
ENST00000683543.2:c.5985A>C	ENSP00000506726.1:p.Gly1995=
ENST00000685166.1:c.5994A>C	ENSP00000509386.1:p.Gly1998=
ENST00000689060.1:c.97A>C
ENST00000689944.1:c.97A>C
ENST00000692637.1:c.5982A>C	ENSP00000509666.1:p.Gly1994=
ENST00000301067.12:c.5985A>C MANE Select	ENSP00000301067.7:p.Gly1995=
ENST00000301067.11:c.5985A>C	ENSP00000301067.7:p.Gly1995=
NM_003482.3:c.5985A>C	NP_003473.3:p.Gly1995=
XM_005269162.3:c.5985A>C	XP_005269219.1:p.Gly1995=
XM_006719614.2:c.5994A>C	XP_006719677.1:p.Gly1998=
XM_006719616.2:c.5982A>C	XP_006719679.1:p.Gly1994=
XM_011538770.1:c.5994A>C	XP_011537072.1:p.Gly1998=
XM_011538771.1:c.5991A>C	XP_011537073.1:p.Gly1997=
XM_011538772.1:c.5985A>C	XP_011537074.1:p.Gly1995=
XM_011538773.1:c.5982A>C	XP_011537075.1:p.Gly1994=
XM_011538774.1:c.5973A>C	XP_011537076.1:p.Gly1991=
XM_011538775.1:c.5994A>C	XP_011537077.1:p.Gly1998=
XM_011538776.1:c.5994A>C	XP_011537078.1:p.Gly1998=
XR_944740.1:n.8314A>C
XM_005269162.4:c.5985A>C	XP_005269219.1:p.Gly1995=
XM_006719614.4:c.5994A>C	XP_006719677.1:p.Gly1998=
XM_006719616.3:c.5982A>C	XP_006719679.1:p.Gly1994=
XM_011538770.2:c.5994A>C	XP_011537072.1:p.Gly1998=
XM_011538771.2:c.5991A>C	XP_011537073.1:p.Gly1997=
XM_011538772.2:c.5985A>C	XP_011537074.1:p.Gly1995=
XM_011538773.2:c.5982A>C	XP_011537075.1:p.Gly1994=
XM_011538774.2:c.5973A>C	XP_011537076.1:p.Gly1991=
XM_011538776.2:c.5994A>C	XP_011537078.1:p.Gly1998=
XR_001748874.1:n.7303A>C
NM_003482.4:c.5985A>C MANE Select	NP_003473.3:p.Gly1995=