Canonical Allele Identifier: CA384717180

Gene: KMT2D

Linked Data

• MyVariant Identifiers: chr12:g.49426878C>G (hg19) ; chr12:g.49033095C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.49033095C>G , CM000674.2:g.49033095C>G	GRCh38
NC_000012.11:g.49426878C>G , CM000674.1:g.49426878C>G	GRCh37
NC_000012.10:g.47713145C>G	NCBI36
NG_027827.1:g.27230G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683543.2:c.11610G>C	ENSP00000506726.1:p.Met3870Ile
ENST00000685166.1:c.11619G>C	ENSP00000509386.1:p.Met3873Ile
ENST00000685554.1:c.1170G>C	ENSP00000508640.1:p.Met390Ile
ENST00000687201.1:c.3189G>C	ENSP00000510037.1:p.Met1063Ile
ENST00000692637.1:c.11607G>C	ENSP00000509666.1:p.Met3869Ile
ENST00000692841.1:c.3089G>C	ENSP00000508711.1:n.3089G>C
ENST00000301067.12:c.11610G>C MANE Select	ENSP00000301067.7:p.Met3870Ile
ENST00000301067.11:c.11610G>C	ENSP00000301067.7:p.Met3870Ile
NM_003482.3:c.11610G>C	NP_003473.3:p.Met3870Ile
XM_005269162.3:c.11610G>C	XP_005269219.1:p.Met3870Ile
XM_006719614.2:c.11619G>C	XP_006719677.1:p.Met3873Ile
XM_006719616.2:c.11607G>C	XP_006719679.1:p.Met3869Ile
XM_011538770.1:c.11619G>C	XP_011537072.1:p.Met3873Ile
XM_011538771.1:c.11616G>C	XP_011537073.1:p.Met3872Ile
XM_011538772.1:c.11610G>C	XP_011537074.1:p.Met3870Ile
XM_011538773.1:c.11607G>C	XP_011537075.1:p.Met3869Ile
XM_011538774.1:c.11598G>C	XP_011537076.1:p.Met3866Ile
XM_011538775.1:c.11619G>C	XP_011537077.1:p.Met3873Ile
XM_011538776.1:c.11526G>C	XP_011537078.1:p.Met3842Ile
XR_944740.1:n.13939G>C
XM_005269162.4:c.11610G>C	XP_005269219.1:p.Met3870Ile
XM_006719614.4:c.11619G>C	XP_006719677.1:p.Met3873Ile
XM_006719616.3:c.11607G>C	XP_006719679.1:p.Met3869Ile
XM_011538770.2:c.11619G>C	XP_011537072.1:p.Met3873Ile
XM_011538771.2:c.11616G>C	XP_011537073.1:p.Met3872Ile
XM_011538772.2:c.11610G>C	XP_011537074.1:p.Met3870Ile
XM_011538773.2:c.11607G>C	XP_011537075.1:p.Met3869Ile
XM_011538774.2:c.11598G>C	XP_011537076.1:p.Met3866Ile
XM_011538776.2:c.11526G>C	XP_011537078.1:p.Met3842Ile
XR_001748874.1:n.12928G>C
NM_003482.4:c.11610G>C MANE Select	NP_003473.3:p.Met3870Ile