Canonical Allele Identifier: CA275138

Gene: KMT2D

Linked Data

• ClinVar Variation Id: 195960
• ClinVar RCV Id: RCV000176652 ; RCV001201615
• dbSNP Id: rs794727420
• gnomAD v4: 12-49042846-G-A
• MyVariant Identifiers: chr12:g.49436629G>A (hg19) ; chr12:g.49042846G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.49042846G>A , CM000674.2:g.49042846G>A	GRCh38
NC_000012.11:g.49436629G>A , CM000674.1:g.49436629G>A	GRCh37
NC_000012.10:g.47722896G>A	NCBI36
NG_027827.1:g.17479C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650290.2:c.489C>T
ENST00000683543.2:c.5677C>T	ENSP00000506726.1:p.Gln1893Ter
ENST00000685166.1:c.5686C>T	ENSP00000509386.1:p.Gln1896Ter
ENST00000688095.1:c.1626C>T	ENSP00000510007.1:n.1626C>T
ENST00000692637.1:c.5674C>T	ENSP00000509666.1:p.Gln1892Ter
ENST00000301067.12:c.5677C>T MANE Select	ENSP00000301067.7:p.Gln1893Ter
ENST00000301067.11:c.5677C>T	ENSP00000301067.7:p.Gln1893Ter
NM_003482.3:c.5677C>T	NP_003473.3:p.Gln1893Ter
XM_005269162.3:c.5677C>T	XP_005269219.1:p.Gln1893Ter
XM_006719614.2:c.5686C>T	XP_006719677.1:p.Gln1896Ter
XM_006719616.2:c.5674C>T	XP_006719679.1:p.Gln1892Ter
XM_011538770.1:c.5686C>T	XP_011537072.1:p.Gln1896Ter
XM_011538771.1:c.5683C>T	XP_011537073.1:p.Gln1895Ter
XM_011538772.1:c.5677C>T	XP_011537074.1:p.Gln1893Ter
XM_011538773.1:c.5674C>T	XP_011537075.1:p.Gln1892Ter
XM_011538774.1:c.5686C>T	XP_011537076.1:p.Gln1896Ter
XM_011538775.1:c.5686C>T	XP_011537077.1:p.Gln1896Ter
XM_011538776.1:c.5686C>T	XP_011537078.1:p.Gln1896Ter
XR_944740.1:n.8006C>T
XM_005269162.4:c.5677C>T	XP_005269219.1:p.Gln1893Ter
XM_006719614.4:c.5686C>T	XP_006719677.1:p.Gln1896Ter
XM_006719616.3:c.5674C>T	XP_006719679.1:p.Gln1892Ter
XM_011538770.2:c.5686C>T	XP_011537072.1:p.Gln1896Ter
XM_011538771.2:c.5683C>T	XP_011537073.1:p.Gln1895Ter
XM_011538772.2:c.5677C>T	XP_011537074.1:p.Gln1893Ter
XM_011538773.2:c.5674C>T	XP_011537075.1:p.Gln1892Ter
XM_011538774.2:c.5686C>T	XP_011537076.1:p.Gln1896Ter
XM_011538776.2:c.5686C>T	XP_011537078.1:p.Gln1896Ter
XR_001748874.1:n.6995C>T
NM_003482.4:c.5677C>T MANE Select	NP_003473.3:p.Gln1893Ter