Canonical Allele Identifier: CA384676224

Gene: KMT2D

Linked Data

• dbSNP Id: rs1942357863
• MyVariant Identifiers: chr12:g.49415903C>G (hg19) ; chr12:g.49022120C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.49022120C>G , CM000674.2:g.49022120C>G	GRCh38
NC_000012.11:g.49415903C>G , CM000674.1:g.49415903C>G	GRCh37
NC_000012.10:g.47702170C>G	NCBI36
NG_027827.1:g.38205G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000526209.2:c.414G>C
ENST00000681974.1:n.1116G>C
ENST00000682693.1:n.2078G>C
ENST00000682886.1:n.850G>C
ENST00000683543.2:c.16492G>C	ENSP00000506726.1:p.Val5498Leu
ENST00000683988.1:c.415G>C	ENSP00000506939.1:p.Val139Leu
ENST00000684428.1:c.1037G>C	ENSP00000507433.1:n.1037G>C
ENST00000685024.1:c.1598G>C
ENST00000685166.1:c.16453G>C	ENSP00000509386.1:p.Val5485Leu
ENST00000691932.1:c.445G>C	ENSP00000509037.1:p.Val149Leu
ENST00000692637.1:c.16441G>C	ENSP00000509666.1:p.Val5481Leu
ENST00000301067.12:c.16444G>C MANE Select	ENSP00000301067.7:p.Val5482Leu
ENST00000301067.11:c.16444G>C	ENSP00000301067.7:p.Val5482Leu
ENST00000526209.1:c.487G>C	ENSP00000435714.1:p.Val163Leu
NM_003482.3:c.16444G>C	NP_003473.3:p.Val5482Leu
XM_005269162.3:c.16444G>C	XP_005269219.1:p.Val5482Leu
XM_006719614.2:c.16453G>C	XP_006719677.1:p.Val5485Leu
XM_006719616.2:c.16441G>C	XP_006719679.1:p.Val5481Leu
XM_011538770.1:c.16501G>C	XP_011537072.1:p.Val5501Leu
XM_011538771.1:c.16498G>C	XP_011537073.1:p.Val5500Leu
XM_011538772.1:c.16492G>C	XP_011537074.1:p.Val5498Leu
XM_011538773.1:c.16489G>C	XP_011537075.1:p.Val5497Leu
XM_011538774.1:c.16480G>C	XP_011537076.1:p.Val5494Leu
XM_011538775.1:c.16435G>C	XP_011537077.1:p.Val5479Leu
XM_011538776.1:c.16408G>C	XP_011537078.1:p.Val5470Leu
XM_005269162.4:c.16444G>C	XP_005269219.1:p.Val5482Leu
XM_006719614.4:c.16453G>C	XP_006719677.1:p.Val5485Leu
XM_006719616.3:c.16441G>C	XP_006719679.1:p.Val5481Leu
XM_011538770.2:c.16501G>C	XP_011537072.1:p.Val5501Leu
XM_011538771.2:c.16498G>C	XP_011537073.1:p.Val5500Leu
XM_011538772.2:c.16492G>C	XP_011537074.1:p.Val5498Leu
XM_011538773.2:c.16489G>C	XP_011537075.1:p.Val5497Leu
XM_011538774.2:c.16480G>C	XP_011537076.1:p.Val5494Leu
XM_011538776.2:c.16408G>C	XP_011537078.1:p.Val5470Leu
XR_001748874.1:n.16621G>C
NM_003482.4:c.16444G>C MANE Select	NP_003473.3:p.Val5482Leu