Canonical Allele Identifier: CA6546598

Gene: KMT2D

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.49037191T>C , CM000674.2:g.49037191T>C	GRCh38
NC_000012.11:g.49430974T>C , CM000674.1:g.49430974T>C	GRCh37
NC_000012.10:g.47717241T>C	NCBI36
NG_027827.1:g.23134A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_003482.4:c.10165A>G MANE Select	NP_003473.3:p.Met3389Val
ENST00000301067.12:c.10165A>G MANE Select	ENSP00000301067.7:p.Met3389Val
NM_003482.3:c.10165A>G	NP_003473.3:p.Met3389Val
ENST00000301067.11:c.10165A>G	ENSP00000301067.7:p.Met3389Val
ENST00000549743.1:n.106A>G
ENST00000683043.1:n.1864A>G
ENST00000683543.2:c.10165A>G	ENSP00000506726.1:p.Met3389Val
ENST00000685166.1:c.10174A>G	ENSP00000509386.1:p.Met3392Val
ENST00000687201.1:c.1729A>G	ENSP00000510037.1:p.Met577Val
ENST00000689143.1:c.3768A>G	ENSP00000509839.1:n.3768A>G
ENST00000692637.1:c.10162A>G	ENSP00000509666.1:p.Met3388Val
ENST00000692841.1:c.1729A>G	ENSP00000508711.1:p.Met577Val
XM_005269162.3:c.10165A>G	XP_005269219.1:p.Met3389Val
XM_005269162.4:c.10165A>G	XP_005269219.1:p.Met3389Val
XM_006719614.2:c.10174A>G	XP_006719677.1:p.Met3392Val
XM_006719614.4:c.10174A>G	XP_006719677.1:p.Met3392Val
XM_006719616.2:c.10162A>G	XP_006719679.1:p.Met3388Val
XM_006719616.3:c.10162A>G	XP_006719679.1:p.Met3388Val
XM_011538770.1:c.10174A>G	XP_011537072.1:p.Met3392Val
XM_011538770.2:c.10174A>G	XP_011537072.1:p.Met3392Val
XM_011538771.1:c.10171A>G	XP_011537073.1:p.Met3391Val
XM_011538771.2:c.10171A>G	XP_011537073.1:p.Met3391Val
XM_011538772.1:c.10165A>G	XP_011537074.1:p.Met3389Val
XM_011538772.2:c.10165A>G	XP_011537074.1:p.Met3389Val
XM_011538773.1:c.10162A>G	XP_011537075.1:p.Met3388Val
XM_011538773.2:c.10162A>G	XP_011537075.1:p.Met3388Val
XM_011538774.1:c.10153A>G	XP_011537076.1:p.Met3385Val
XM_011538774.2:c.10153A>G	XP_011537076.1:p.Met3385Val
XM_011538775.1:c.10174A>G	XP_011537077.1:p.Met3392Val
XM_011538776.1:c.10081A>G	XP_011537078.1:p.Met3361Val
XM_011538776.2:c.10081A>G	XP_011537078.1:p.Met3361Val
XR_001748874.1:n.11483A>G
XR_944740.1:n.12494A>G