Canonical Allele Identifier: CA384676405

Gene: KMT2D

Linked Data

• dbSNP Id: rs2137704017
• MyVariant Identifiers: chr12:g.49415918A>G (hg19) ; chr12:g.49022135A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.49022135A>G , CM000674.2:g.49022135A>G	GRCh38
NC_000012.11:g.49415918A>G , CM000674.1:g.49415918A>G	GRCh37
NC_000012.10:g.47702185A>G	NCBI36
NG_027827.1:g.38190T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000526209.2:c.399T>C
ENST00000681974.1:n.1101T>C
ENST00000682693.1:n.2063T>C
ENST00000682886.1:n.835T>C
ENST00000683543.2:c.16477T>C	ENSP00000506726.1:p.Cys5493Arg
ENST00000683988.1:c.400T>C	ENSP00000506939.1:p.Cys134Arg
ENST00000684428.1:c.1022T>C	ENSP00000507433.1:n.1022T>C
ENST00000685024.1:c.1583T>C
ENST00000685166.1:c.16438T>C	ENSP00000509386.1:p.Cys5480Arg
ENST00000691932.1:c.430T>C	ENSP00000509037.1:p.Cys144Arg
ENST00000692637.1:c.16426T>C	ENSP00000509666.1:p.Cys5476Arg
ENST00000301067.12:c.16429T>C MANE Select	ENSP00000301067.7:p.Cys5477Arg
ENST00000301067.11:c.16429T>C	ENSP00000301067.7:p.Cys5477Arg
ENST00000526209.1:c.472T>C	ENSP00000435714.1:p.Cys158Arg
NM_003482.3:c.16429T>C	NP_003473.3:p.Cys5477Arg
XM_005269162.3:c.16429T>C	XP_005269219.1:p.Cys5477Arg
XM_006719614.2:c.16438T>C	XP_006719677.1:p.Cys5480Arg
XM_006719616.2:c.16426T>C	XP_006719679.1:p.Cys5476Arg
XM_011538770.1:c.16486T>C	XP_011537072.1:p.Cys5496Arg
XM_011538771.1:c.16483T>C	XP_011537073.1:p.Cys5495Arg
XM_011538772.1:c.16477T>C	XP_011537074.1:p.Cys5493Arg
XM_011538773.1:c.16474T>C	XP_011537075.1:p.Cys5492Arg
XM_011538774.1:c.16465T>C	XP_011537076.1:p.Cys5489Arg
XM_011538775.1:c.16420T>C	XP_011537077.1:p.Cys5474Arg
XM_011538776.1:c.16393T>C	XP_011537078.1:p.Cys5465Arg
XM_005269162.4:c.16429T>C	XP_005269219.1:p.Cys5477Arg
XM_006719614.4:c.16438T>C	XP_006719677.1:p.Cys5480Arg
XM_006719616.3:c.16426T>C	XP_006719679.1:p.Cys5476Arg
XM_011538770.2:c.16486T>C	XP_011537072.1:p.Cys5496Arg
XM_011538771.2:c.16483T>C	XP_011537073.1:p.Cys5495Arg
XM_011538772.2:c.16477T>C	XP_011537074.1:p.Cys5493Arg
XM_011538773.2:c.16474T>C	XP_011537075.1:p.Cys5492Arg
XM_011538774.2:c.16465T>C	XP_011537076.1:p.Cys5489Arg
XM_011538776.2:c.16393T>C	XP_011537078.1:p.Cys5465Arg
XR_001748874.1:n.16606T>C
NM_003482.4:c.16429T>C MANE Select	NP_003473.3:p.Cys5477Arg