Canonical Allele Identifier: CA384743638

Gene: KMT2D

Linked Data

• dbSNP Id: rs1355857425
• MyVariant Identifiers: chr12:g.49433282G>C (hg19) ; chr12:g.49039499G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.49039499G>C , CM000674.2:g.49039499G>C	GRCh38
NC_000012.11:g.49433282G>C , CM000674.1:g.49433282G>C	GRCh37
NC_000012.10:g.47719549G>C	NCBI36
NG_027827.1:g.20826C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683543.2:c.8165C>G	ENSP00000506726.1:p.Ala2722Gly
ENST00000685166.1:c.8174C>G	ENSP00000509386.1:p.Ala2725Gly
ENST00000689060.1:c.2184C>G
ENST00000689143.1:c.1838C>G	ENSP00000509839.1:p.Ala613Gly
ENST00000689944.1:c.2274C>G
ENST00000692637.1:c.8162C>G	ENSP00000509666.1:p.Ala2721Gly
ENST00000301067.12:c.8165C>G MANE Select	ENSP00000301067.7:p.Ala2722Gly
ENST00000301067.11:c.8165C>G	ENSP00000301067.7:p.Ala2722Gly
NM_003482.3:c.8165C>G	NP_003473.3:p.Ala2722Gly
XM_005269162.3:c.8165C>G	XP_005269219.1:p.Ala2722Gly
XM_006719614.2:c.8174C>G	XP_006719677.1:p.Ala2725Gly
XM_006719616.2:c.8162C>G	XP_006719679.1:p.Ala2721Gly
XM_011538770.1:c.8174C>G	XP_011537072.1:p.Ala2725Gly
XM_011538771.1:c.8171C>G	XP_011537073.1:p.Ala2724Gly
XM_011538772.1:c.8165C>G	XP_011537074.1:p.Ala2722Gly
XM_011538773.1:c.8162C>G	XP_011537075.1:p.Ala2721Gly
XM_011538774.1:c.8153C>G	XP_011537076.1:p.Ala2718Gly
XM_011538775.1:c.8174C>G	XP_011537077.1:p.Ala2725Gly
XM_011538776.1:c.8081C>G	XP_011537078.1:p.Ala2694Gly
XR_944740.1:n.10494C>G
XM_005269162.4:c.8165C>G	XP_005269219.1:p.Ala2722Gly
XM_006719614.4:c.8174C>G	XP_006719677.1:p.Ala2725Gly
XM_006719616.3:c.8162C>G	XP_006719679.1:p.Ala2721Gly
XM_011538770.2:c.8174C>G	XP_011537072.1:p.Ala2725Gly
XM_011538771.2:c.8171C>G	XP_011537073.1:p.Ala2724Gly
XM_011538772.2:c.8165C>G	XP_011537074.1:p.Ala2722Gly
XM_011538773.2:c.8162C>G	XP_011537075.1:p.Ala2721Gly
XM_011538774.2:c.8153C>G	XP_011537076.1:p.Ala2718Gly
XM_011538776.2:c.8081C>G	XP_011537078.1:p.Ala2694Gly
XR_001748874.1:n.9483C>G
NM_003482.4:c.8165C>G MANE Select	NP_003473.3:p.Ala2722Gly