Canonical Allele Identifier: CA2618605349

Gene: KMT2D

Linked Data

• dbSNP Id: rs2137704721
• gnomAD v4: 12-49022269-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.49022269T>C , CM000674.2:g.49022269T>C	GRCh38
NC_000012.11:g.49416052T>C , CM000674.1:g.49416052T>C	GRCh37
NC_000012.10:g.47702319T>C	NCBI36
NG_027827.1:g.38056A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000526209.2:c.382+11A>G
ENST00000681974.1:n.1084+11A>G
ENST00000682693.1:n.2046+11A>G
ENST00000682886.1:n.818+11A>G
ENST00000683543.2:c.16460+11A>G	ENSP00000506726.1:n.16460+11A>G
ENST00000683988.1:c.383+11A>G	ENSP00000506939.1:n.383+11A>G
ENST00000684428.1:c.1005+11A>G	ENSP00000507433.1:n.1005+11A>G
ENST00000685024.1:c.1566+11A>G
ENST00000685166.1:c.16421+11A>G	ENSP00000509386.1:n.16421+11A>G
ENST00000691932.1:c.413+11A>G	ENSP00000509037.1:n.413+11A>G
ENST00000692637.1:c.16409+11A>G	ENSP00000509666.1:n.16409+11A>G
ENST00000301067.12:c.16412+11A>G MANE Select	ENSP00000301067.7:n.16412+11A>G
ENST00000301067.11:c.16412+11A>G	ENSP00000301067.7:n.16412+11A>G
ENST00000526209.1:c.455+11A>G	ENSP00000435714.1:n.455+11A>G
NM_003482.3:c.16412+11A>G	NP_003473.3:n.16412+11A>G
XM_005269162.3:c.16412+11A>G	XP_005269219.1:n.16412+11A>G
XM_006719614.2:c.16421+11A>G	XP_006719677.1:n.16421+11A>G
XM_006719616.2:c.16409+11A>G	XP_006719679.1:n.16409+11A>G
XM_011538770.1:c.16469+11A>G	XP_011537072.1:n.16469+11A>G
XM_011538771.1:c.16466+11A>G	XP_011537073.1:n.16466+11A>G
XM_011538772.1:c.16460+11A>G	XP_011537074.1:n.16460+11A>G
XM_011538773.1:c.16457+11A>G	XP_011537075.1:n.16457+11A>G
XM_011538774.1:c.16448+11A>G	XP_011537076.1:n.16448+11A>G
XM_011538775.1:c.16403+11A>G	XP_011537077.1:n.16403+11A>G
XM_011538776.1:c.16376+11A>G	XP_011537078.1:n.16376+11A>G
XM_005269162.4:c.16412+11A>G	XP_005269219.1:n.16412+11A>G
XM_006719614.4:c.16421+11A>G	XP_006719677.1:n.16421+11A>G
XM_006719616.3:c.16409+11A>G	XP_006719679.1:n.16409+11A>G
XM_011538770.2:c.16469+11A>G	XP_011537072.1:n.16469+11A>G
XM_011538771.2:c.16466+11A>G	XP_011537073.1:n.16466+11A>G
XM_011538772.2:c.16460+11A>G	XP_011537074.1:n.16460+11A>G
XM_011538773.2:c.16457+11A>G	XP_011537075.1:n.16457+11A>G
XM_011538774.2:c.16448+11A>G	XP_011537076.1:n.16448+11A>G
XM_011538776.2:c.16376+11A>G	XP_011537078.1:n.16376+11A>G
XR_001748874.1:n.16589+11A>G
NM_003482.4:c.16412+11A>G MANE Select	NP_003473.3:n.16412+11A>G