Canonical Allele Identifier: CA384681429

Gene: KMT2D

Linked Data

• MyVariant Identifiers: chr12:g.49418416T>C (hg19) ; chr12:g.49024633T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.49024633T>C , CM000674.2:g.49024633T>C	GRCh38
NC_000012.11:g.49418416T>C , CM000674.1:g.49418416T>C	GRCh37
NC_000012.10:g.47704683T>C	NCBI36
NG_027827.1:g.35692A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000681974.1:n.669A>G
ENST00000683543.2:c.15997A>G	ENSP00000506726.1:p.Ile5333Val
ENST00000683863.1:n.1712A>G
ENST00000684428.1:c.532A>G	ENSP00000507433.1:p.Ile178Val
ENST00000684755.1:n.532A>G
ENST00000685024.1:c.1151A>G
ENST00000685166.1:c.16006A>G	ENSP00000509386.1:p.Ile5336Val
ENST00000688411.1:c.474A>G	ENSP00000510146.1:n.474A>G
ENST00000691932.1:c.76A>G	ENSP00000509037.1:p.Ile26Val
ENST00000692637.1:c.15994A>G	ENSP00000509666.1:p.Ile5332Val
ENST00000301067.12:c.15997A>G MANE Select	ENSP00000301067.7:p.Ile5333Val
ENST00000301067.11:c.15997A>G	ENSP00000301067.7:p.Ile5333Val
NM_003482.3:c.15997A>G	NP_003473.3:p.Ile5333Val
XM_005269162.3:c.15997A>G	XP_005269219.1:p.Ile5333Val
XM_006719614.2:c.16006A>G	XP_006719677.1:p.Ile5336Val
XM_006719616.2:c.15994A>G	XP_006719679.1:p.Ile5332Val
XM_011538770.1:c.16006A>G	XP_011537072.1:p.Ile5336Val
XM_011538771.1:c.16003A>G	XP_011537073.1:p.Ile5335Val
XM_011538772.1:c.15997A>G	XP_011537074.1:p.Ile5333Val
XM_011538773.1:c.15994A>G	XP_011537075.1:p.Ile5332Val
XM_011538774.1:c.15985A>G	XP_011537076.1:p.Ile5329Val
XM_011538775.1:c.15940A>G	XP_011537077.1:p.Ile5314Val
XM_011538776.1:c.15913A>G	XP_011537078.1:p.Ile5305Val
XM_005269162.4:c.15997A>G	XP_005269219.1:p.Ile5333Val
XM_006719614.4:c.16006A>G	XP_006719677.1:p.Ile5336Val
XM_006719616.3:c.15994A>G	XP_006719679.1:p.Ile5332Val
XM_011538770.2:c.16006A>G	XP_011537072.1:p.Ile5336Val
XM_011538771.2:c.16003A>G	XP_011537073.1:p.Ile5335Val
XM_011538772.2:c.15997A>G	XP_011537074.1:p.Ile5333Val
XM_011538773.2:c.15994A>G	XP_011537075.1:p.Ile5332Val
XM_011538774.2:c.15985A>G	XP_011537076.1:p.Ile5329Val
XM_011538776.2:c.15913A>G	XP_011537078.1:p.Ile5305Val
XR_001748874.1:n.16174A>G
NM_003482.4:c.15997A>G MANE Select	NP_003473.3:p.Ile5333Val