Canonical Allele Identifier: CA479708785

Gene: KMT2D

Linked Data

• dbSNP Id: rs1162211851
• MyVariant Identifiers: chr12:g.49426821C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.49033038C>A , CM000674.2:g.49033038C>A	GRCh38
NC_000012.11:g.49426821C>A , CM000674.1:g.49426821C>A	GRCh37
NC_000012.10:g.47713088C>A	NCBI36
NG_027827.1:g.27287G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683543.2:c.11667G>T	ENSP00000506726.1:p.Leu3889=
ENST00000685166.1:c.11676G>T	ENSP00000509386.1:p.Leu3892=
ENST00000685554.1:c.1227G>T	ENSP00000508640.1:p.Leu409=
ENST00000687201.1:c.3246G>T	ENSP00000510037.1:p.Leu1082=
ENST00000692637.1:c.11664G>T	ENSP00000509666.1:p.Leu3888=
ENST00000692841.1:c.3146G>T	ENSP00000508711.1:n.3146G>T
ENST00000301067.12:c.11667G>T MANE Select	ENSP00000301067.7:p.Leu3889=
ENST00000301067.11:c.11667G>T	ENSP00000301067.7:p.Leu3889=
NM_003482.3:c.11667G>T	NP_003473.3:p.Leu3889=
XM_005269162.3:c.11667G>T	XP_005269219.1:p.Leu3889=
XM_006719614.2:c.11676G>T	XP_006719677.1:p.Leu3892=
XM_006719616.2:c.11664G>T	XP_006719679.1:p.Leu3888=
XM_011538770.1:c.11676G>T	XP_011537072.1:p.Leu3892=
XM_011538771.1:c.11673G>T	XP_011537073.1:p.Leu3891=
XM_011538772.1:c.11667G>T	XP_011537074.1:p.Leu3889=
XM_011538773.1:c.11664G>T	XP_011537075.1:p.Leu3888=
XM_011538774.1:c.11655G>T	XP_011537076.1:p.Leu3885=
XM_011538775.1:c.11676G>T	XP_011537077.1:p.Leu3892=
XM_011538776.1:c.11583G>T	XP_011537078.1:p.Leu3861=
XR_944740.1:n.13996G>T
XM_005269162.4:c.11667G>T	XP_005269219.1:p.Leu3889=
XM_006719614.4:c.11676G>T	XP_006719677.1:p.Leu3892=
XM_006719616.3:c.11664G>T	XP_006719679.1:p.Leu3888=
XM_011538770.2:c.11676G>T	XP_011537072.1:p.Leu3892=
XM_011538771.2:c.11673G>T	XP_011537073.1:p.Leu3891=
XM_011538772.2:c.11667G>T	XP_011537074.1:p.Leu3889=
XM_011538773.2:c.11664G>T	XP_011537075.1:p.Leu3888=
XM_011538774.2:c.11655G>T	XP_011537076.1:p.Leu3885=
XM_011538776.2:c.11583G>T	XP_011537078.1:p.Leu3861=
XR_001748874.1:n.12985G>T
NM_003482.4:c.11667G>T MANE Select	NP_003473.3:p.Leu3889=