Canonical Allele Identifier: CA479521998

Gene: KMT2D

Linked Data

• MyVariant Identifiers: chr12:g.49418617A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.49024834A>G , CM000674.2:g.49024834A>G	GRCh38
NC_000012.11:g.49418617A>G , CM000674.1:g.49418617A>G	GRCh37
NC_000012.10:g.47704884A>G	NCBI36
NG_027827.1:g.35491T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000681974.1:n.569T>C
ENST00000683543.2:c.15897T>C	ENSP00000506726.1:p.His5299=
ENST00000683863.1:n.1612T>C
ENST00000684428.1:c.432T>C	ENSP00000507433.1:p.His144=
ENST00000684755.1:n.432T>C
ENST00000685024.1:c.1022T>C
ENST00000685166.1:c.15906T>C	ENSP00000509386.1:p.His5302=
ENST00000688411.1:c.374T>C	ENSP00000510146.1:n.374T>C
ENST00000691463.1:c.1283T>C	ENSP00000510624.1:n.1283T>C
ENST00000692637.1:c.15894T>C	ENSP00000509666.1:p.His5298=
ENST00000301067.12:c.15897T>C MANE Select	ENSP00000301067.7:p.His5299=
ENST00000301067.11:c.15897T>C	ENSP00000301067.7:p.His5299=
NM_003482.3:c.15897T>C	NP_003473.3:p.His5299=
XM_005269162.3:c.15897T>C	XP_005269219.1:p.His5299=
XM_006719614.2:c.15906T>C	XP_006719677.1:p.His5302=
XM_006719616.2:c.15894T>C	XP_006719679.1:p.His5298=
XM_011538770.1:c.15906T>C	XP_011537072.1:p.His5302=
XM_011538771.1:c.15903T>C	XP_011537073.1:p.His5301=
XM_011538772.1:c.15897T>C	XP_011537074.1:p.His5299=
XM_011538773.1:c.15894T>C	XP_011537075.1:p.His5298=
XM_011538774.1:c.15885T>C	XP_011537076.1:p.His5295=
XM_011538775.1:c.15840T>C	XP_011537077.1:p.His5280=
XM_011538776.1:c.15813T>C	XP_011537078.1:p.His5271=
XR_944740.1:n.17085T>C
XM_005269162.4:c.15897T>C	XP_005269219.1:p.His5299=
XM_006719614.4:c.15906T>C	XP_006719677.1:p.His5302=
XM_006719616.3:c.15894T>C	XP_006719679.1:p.His5298=
XM_011538770.2:c.15906T>C	XP_011537072.1:p.His5302=
XM_011538771.2:c.15903T>C	XP_011537073.1:p.His5301=
XM_011538772.2:c.15897T>C	XP_011537074.1:p.His5299=
XM_011538773.2:c.15894T>C	XP_011537075.1:p.His5298=
XM_011538774.2:c.15885T>C	XP_011537076.1:p.His5295=
XM_011538776.2:c.15813T>C	XP_011537078.1:p.His5271=
XR_001748874.1:n.16074T>C
NM_003482.4:c.15897T>C MANE Select	NP_003473.3:p.His5299=