Canonical Allele Identifier: CA479521074

Gene: KMT2D

Linked Data

• dbSNP Id: rs2137706418
• MyVariant Identifiers: chr12:g.49416421G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.49022638G>A , CM000674.2:g.49022638G>A	GRCh38
NC_000012.11:g.49416421G>A , CM000674.1:g.49416421G>A	GRCh37
NC_000012.10:g.47702688G>A	NCBI36
NG_027827.1:g.37687C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000526209.2:c.260C>T
ENST00000681974.1:n.962C>T
ENST00000682693.1:n.1924C>T
ENST00000682886.1:n.460C>T
ENST00000683543.2:c.16338C>T	ENSP00000506726.1:p.Ile5446=
ENST00000683988.1:c.261C>T	ENSP00000506939.1:p.Ile87=
ENST00000684428.1:c.825C>T	ENSP00000507433.1:p.Ile275=
ENST00000684755.1:n.873C>T
ENST00000685024.1:c.1444C>T
ENST00000685166.1:c.16299C>T	ENSP00000509386.1:p.Ile5433=
ENST00000688411.1:c.767C>T	ENSP00000510146.1:n.767C>T
ENST00000691932.1:c.291C>T	ENSP00000509037.1:p.Ile97=
ENST00000692637.1:c.16287C>T	ENSP00000509666.1:p.Ile5429=
ENST00000301067.12:c.16290C>T MANE Select	ENSP00000301067.7:p.Ile5430=
ENST00000301067.11:c.16290C>T	ENSP00000301067.7:p.Ile5430=
ENST00000526209.1:c.333C>T	ENSP00000435714.1:p.Ile111=
NM_003482.3:c.16290C>T	NP_003473.3:p.Ile5430=
XM_005269162.3:c.16290C>T	XP_005269219.1:p.Ile5430=
XM_006719614.2:c.16299C>T	XP_006719677.1:p.Ile5433=
XM_006719616.2:c.16287C>T	XP_006719679.1:p.Ile5429=
XM_011538770.1:c.16347C>T	XP_011537072.1:p.Ile5449=
XM_011538771.1:c.16344C>T	XP_011537073.1:p.Ile5448=
XM_011538772.1:c.16338C>T	XP_011537074.1:p.Ile5446=
XM_011538773.1:c.16335C>T	XP_011537075.1:p.Ile5445=
XM_011538774.1:c.16326C>T	XP_011537076.1:p.Ile5442=
XM_011538775.1:c.16281C>T	XP_011537077.1:p.Ile5427=
XM_011538776.1:c.16254C>T	XP_011537078.1:p.Ile5418=
XM_005269162.4:c.16290C>T	XP_005269219.1:p.Ile5430=
XM_006719614.4:c.16299C>T	XP_006719677.1:p.Ile5433=
XM_006719616.3:c.16287C>T	XP_006719679.1:p.Ile5429=
XM_011538770.2:c.16347C>T	XP_011537072.1:p.Ile5449=
XM_011538771.2:c.16344C>T	XP_011537073.1:p.Ile5448=
XM_011538772.2:c.16338C>T	XP_011537074.1:p.Ile5446=
XM_011538773.2:c.16335C>T	XP_011537075.1:p.Ile5445=
XM_011538774.2:c.16326C>T	XP_011537076.1:p.Ile5442=
XM_011538776.2:c.16254C>T	XP_011537078.1:p.Ile5418=
XR_001748874.1:n.16467C>T
NM_003482.4:c.16290C>T MANE Select	NP_003473.3:p.Ile5430=