Canonical Allele Identifier: CA384743772

Gene: KMT2D

Linked Data

• MyVariant Identifiers: chr12:g.49433297G>T (hg19) ; chr12:g.49039514G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.49039514G>T , CM000674.2:g.49039514G>T	GRCh38
NC_000012.11:g.49433297G>T , CM000674.1:g.49433297G>T	GRCh37
NC_000012.10:g.47719564G>T	NCBI36
NG_027827.1:g.20811C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683543.2:c.8150C>A	ENSP00000506726.1:p.Pro2717Gln
ENST00000685166.1:c.8159C>A	ENSP00000509386.1:p.Pro2720Gln
ENST00000689060.1:c.2169C>A
ENST00000689143.1:c.1823C>A	ENSP00000509839.1:p.Pro608Gln
ENST00000689944.1:c.2259C>A
ENST00000692637.1:c.8147C>A	ENSP00000509666.1:p.Pro2716Gln
ENST00000301067.12:c.8150C>A MANE Select	ENSP00000301067.7:p.Pro2717Gln
ENST00000301067.11:c.8150C>A	ENSP00000301067.7:p.Pro2717Gln
NM_003482.3:c.8150C>A	NP_003473.3:p.Pro2717Gln
XM_005269162.3:c.8150C>A	XP_005269219.1:p.Pro2717Gln
XM_006719614.2:c.8159C>A	XP_006719677.1:p.Pro2720Gln
XM_006719616.2:c.8147C>A	XP_006719679.1:p.Pro2716Gln
XM_011538770.1:c.8159C>A	XP_011537072.1:p.Pro2720Gln
XM_011538771.1:c.8156C>A	XP_011537073.1:p.Pro2719Gln
XM_011538772.1:c.8150C>A	XP_011537074.1:p.Pro2717Gln
XM_011538773.1:c.8147C>A	XP_011537075.1:p.Pro2716Gln
XM_011538774.1:c.8138C>A	XP_011537076.1:p.Pro2713Gln
XM_011538775.1:c.8159C>A	XP_011537077.1:p.Pro2720Gln
XM_011538776.1:c.8066C>A	XP_011537078.1:p.Pro2689Gln
XR_944740.1:n.10479C>A
XM_005269162.4:c.8150C>A	XP_005269219.1:p.Pro2717Gln
XM_006719614.4:c.8159C>A	XP_006719677.1:p.Pro2720Gln
XM_006719616.3:c.8147C>A	XP_006719679.1:p.Pro2716Gln
XM_011538770.2:c.8159C>A	XP_011537072.1:p.Pro2720Gln
XM_011538771.2:c.8156C>A	XP_011537073.1:p.Pro2719Gln
XM_011538772.2:c.8150C>A	XP_011537074.1:p.Pro2717Gln
XM_011538773.2:c.8147C>A	XP_011537075.1:p.Pro2716Gln
XM_011538774.2:c.8138C>A	XP_011537076.1:p.Pro2713Gln
XM_011538776.2:c.8066C>A	XP_011537078.1:p.Pro2689Gln
XR_001748874.1:n.9468C>A
NM_003482.4:c.8150C>A MANE Select	NP_003473.3:p.Pro2717Gln