Canonical Allele Identifier: CA384703393

Gene: KMT2D

Linked Data

• dbSNP Id: rs2120412140
• gnomAD v4: 12-49030951-T-C
• MyVariant Identifiers: chr12:g.49424734T>C (hg19) ; chr12:g.49030951T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.49030951T>C , CM000674.2:g.49030951T>C	GRCh38
NC_000012.11:g.49424734T>C , CM000674.1:g.49424734T>C	GRCh37
NC_000012.10:g.47711001T>C	NCBI36
NG_027827.1:g.29374A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000552391.2:n.313A>G
ENST00000683543.2:c.13613A>G	ENSP00000506726.1:p.Lys4538Arg
ENST00000685166.1:c.13622A>G	ENSP00000509386.1:p.Lys4541Arg
ENST00000685982.1:c.139-183A>G	ENSP00000508613.1:n.139-183A>G
ENST00000691986.1:c.138+224A>G	ENSP00000509196.1:n.138+224A>G
ENST00000692637.1:c.13610A>G	ENSP00000509666.1:p.Lys4537Arg
ENST00000692973.1:c.214A>G	ENSP00000508893.1:n.214A>G
ENST00000301067.12:c.13613A>G MANE Select	ENSP00000301067.7:p.Lys4538Arg
ENST00000301067.11:c.13613A>G	ENSP00000301067.7:p.Lys4538Arg
ENST00000552391.1:n.313A>G
NM_003482.3:c.13613A>G	NP_003473.3:p.Lys4538Arg
XM_005269162.3:c.13613A>G	XP_005269219.1:p.Lys4538Arg
XM_006719614.2:c.13622A>G	XP_006719677.1:p.Lys4541Arg
XM_006719616.2:c.13610A>G	XP_006719679.1:p.Lys4537Arg
XM_011538770.1:c.13622A>G	XP_011537072.1:p.Lys4541Arg
XM_011538771.1:c.13619A>G	XP_011537073.1:p.Lys4540Arg
XM_011538772.1:c.13613A>G	XP_011537074.1:p.Lys4538Arg
XM_011538773.1:c.13610A>G	XP_011537075.1:p.Lys4537Arg
XM_011538774.1:c.13601A>G	XP_011537076.1:p.Lys4534Arg
XM_011538775.1:c.13622A>G	XP_011537077.1:p.Lys4541Arg
XM_011538776.1:c.13529A>G	XP_011537078.1:p.Lys4510Arg
XR_944740.1:n.15942A>G
XM_005269162.4:c.13613A>G	XP_005269219.1:p.Lys4538Arg
XM_006719614.4:c.13622A>G	XP_006719677.1:p.Lys4541Arg
XM_006719616.3:c.13610A>G	XP_006719679.1:p.Lys4537Arg
XM_011538770.2:c.13622A>G	XP_011537072.1:p.Lys4541Arg
XM_011538771.2:c.13619A>G	XP_011537073.1:p.Lys4540Arg
XM_011538772.2:c.13613A>G	XP_011537074.1:p.Lys4538Arg
XM_011538773.2:c.13610A>G	XP_011537075.1:p.Lys4537Arg
XM_011538774.2:c.13601A>G	XP_011537076.1:p.Lys4534Arg
XM_011538776.2:c.13529A>G	XP_011537078.1:p.Lys4510Arg
XR_001748874.1:n.14931A>G
NM_003482.4:c.13613A>G MANE Select	NP_003473.3:p.Lys4538Arg