Canonical Allele Identifier: CA384681780

Gene: KMT2D

Linked Data

• MyVariant Identifiers: chr12:g.49418452A>G (hg19) ; chr12:g.49024669A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.49024669A>G , CM000674.2:g.49024669A>G	GRCh38
NC_000012.11:g.49418452A>G , CM000674.1:g.49418452A>G	GRCh37
NC_000012.10:g.47704719A>G	NCBI36
NG_027827.1:g.35656T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000681974.1:n.633T>C
ENST00000683543.2:c.15961T>C	ENSP00000506726.1:p.Tyr5321His
ENST00000683863.1:n.1676T>C
ENST00000684428.1:c.496T>C	ENSP00000507433.1:p.Tyr166His
ENST00000684755.1:n.496T>C
ENST00000685024.1:c.1115T>C
ENST00000685166.1:c.15970T>C	ENSP00000509386.1:p.Tyr5324His
ENST00000688411.1:c.438T>C	ENSP00000510146.1:n.438T>C
ENST00000691932.1:c.40T>C	ENSP00000509037.1:p.Tyr14His
ENST00000692637.1:c.15958T>C	ENSP00000509666.1:p.Tyr5320His
ENST00000301067.12:c.15961T>C MANE Select	ENSP00000301067.7:p.Tyr5321His
ENST00000301067.11:c.15961T>C	ENSP00000301067.7:p.Tyr5321His
NM_003482.3:c.15961T>C	NP_003473.3:p.Tyr5321His
XM_005269162.3:c.15961T>C	XP_005269219.1:p.Tyr5321His
XM_006719614.2:c.15970T>C	XP_006719677.1:p.Tyr5324His
XM_006719616.2:c.15958T>C	XP_006719679.1:p.Tyr5320His
XM_011538770.1:c.15970T>C	XP_011537072.1:p.Tyr5324His
XM_011538771.1:c.15967T>C	XP_011537073.1:p.Tyr5323His
XM_011538772.1:c.15961T>C	XP_011537074.1:p.Tyr5321His
XM_011538773.1:c.15958T>C	XP_011537075.1:p.Tyr5320His
XM_011538774.1:c.15949T>C	XP_011537076.1:p.Tyr5317His
XM_011538775.1:c.15904T>C	XP_011537077.1:p.Tyr5302His
XM_011538776.1:c.15877T>C	XP_011537078.1:p.Tyr5293His
XM_005269162.4:c.15961T>C	XP_005269219.1:p.Tyr5321His
XM_006719614.4:c.15970T>C	XP_006719677.1:p.Tyr5324His
XM_006719616.3:c.15958T>C	XP_006719679.1:p.Tyr5320His
XM_011538770.2:c.15970T>C	XP_011537072.1:p.Tyr5324His
XM_011538771.2:c.15967T>C	XP_011537073.1:p.Tyr5323His
XM_011538772.2:c.15961T>C	XP_011537074.1:p.Tyr5321His
XM_011538773.2:c.15958T>C	XP_011537075.1:p.Tyr5320His
XM_011538774.2:c.15949T>C	XP_011537076.1:p.Tyr5317His
XM_011538776.2:c.15877T>C	XP_011537078.1:p.Tyr5293His
XR_001748874.1:n.16138T>C
NM_003482.4:c.15961T>C MANE Select	NP_003473.3:p.Tyr5321His