Canonical Allele Identifier: CA384743409

Gene: KMT2D

Linked Data

• dbSNP Id: rs1279860885
• MyVariant Identifiers: chr12:g.49433253G>T (hg19) ; chr12:g.49039470G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.49039470G>T , CM000674.2:g.49039470G>T	GRCh38
NC_000012.11:g.49433253G>T , CM000674.1:g.49433253G>T	GRCh37
NC_000012.10:g.47719520G>T	NCBI36
NG_027827.1:g.20855C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683543.2:c.8194C>A	ENSP00000506726.1:p.Leu2732Met
ENST00000685166.1:c.8203C>A	ENSP00000509386.1:p.Leu2735Met
ENST00000689060.1:c.2213C>A
ENST00000689143.1:c.1867C>A	ENSP00000509839.1:p.Leu623Met
ENST00000689944.1:c.2303C>A
ENST00000692637.1:c.8191C>A	ENSP00000509666.1:p.Leu2731Met
ENST00000301067.12:c.8194C>A MANE Select	ENSP00000301067.7:p.Leu2732Met
ENST00000301067.11:c.8194C>A	ENSP00000301067.7:p.Leu2732Met
NM_003482.3:c.8194C>A	NP_003473.3:p.Leu2732Met
XM_005269162.3:c.8194C>A	XP_005269219.1:p.Leu2732Met
XM_006719614.2:c.8203C>A	XP_006719677.1:p.Leu2735Met
XM_006719616.2:c.8191C>A	XP_006719679.1:p.Leu2731Met
XM_011538770.1:c.8203C>A	XP_011537072.1:p.Leu2735Met
XM_011538771.1:c.8200C>A	XP_011537073.1:p.Leu2734Met
XM_011538772.1:c.8194C>A	XP_011537074.1:p.Leu2732Met
XM_011538773.1:c.8191C>A	XP_011537075.1:p.Leu2731Met
XM_011538774.1:c.8182C>A	XP_011537076.1:p.Leu2728Met
XM_011538775.1:c.8203C>A	XP_011537077.1:p.Leu2735Met
XM_011538776.1:c.8110C>A	XP_011537078.1:p.Leu2704Met
XR_944740.1:n.10523C>A
XM_005269162.4:c.8194C>A	XP_005269219.1:p.Leu2732Met
XM_006719614.4:c.8203C>A	XP_006719677.1:p.Leu2735Met
XM_006719616.3:c.8191C>A	XP_006719679.1:p.Leu2731Met
XM_011538770.2:c.8203C>A	XP_011537072.1:p.Leu2735Met
XM_011538771.2:c.8200C>A	XP_011537073.1:p.Leu2734Met
XM_011538772.2:c.8194C>A	XP_011537074.1:p.Leu2732Met
XM_011538773.2:c.8191C>A	XP_011537075.1:p.Leu2731Met
XM_011538774.2:c.8182C>A	XP_011537076.1:p.Leu2728Met
XM_011538776.2:c.8110C>A	XP_011537078.1:p.Leu2704Met
XR_001748874.1:n.9512C>A
NM_003482.4:c.8194C>A MANE Select	NP_003473.3:p.Leu2732Met