Canonical Allele Identifier: CA384681403

Gene: KMT2D

Linked Data

• MyVariant Identifiers: chr12:g.49418412T>G (hg19) ; chr12:g.49024629T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.49024629T>G , CM000674.2:g.49024629T>G	GRCh38
NC_000012.11:g.49418412T>G , CM000674.1:g.49418412T>G	GRCh37
NC_000012.10:g.47704679T>G	NCBI36
NG_027827.1:g.35696A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000681974.1:n.673A>C
ENST00000683543.2:c.16001A>C	ENSP00000506726.1:p.Asn5334Thr
ENST00000683863.1:n.1716A>C
ENST00000684428.1:c.536A>C	ENSP00000507433.1:p.Asn179Thr
ENST00000684755.1:n.536A>C
ENST00000685024.1:c.1155A>C
ENST00000685166.1:c.16010A>C	ENSP00000509386.1:p.Asn5337Thr
ENST00000688411.1:c.478A>C	ENSP00000510146.1:n.478A>C
ENST00000691932.1:c.80A>C	ENSP00000509037.1:p.Asn27Thr
ENST00000692637.1:c.15998A>C	ENSP00000509666.1:p.Asn5333Thr
ENST00000301067.12:c.16001A>C MANE Select	ENSP00000301067.7:p.Asn5334Thr
ENST00000301067.11:c.16001A>C	ENSP00000301067.7:p.Asn5334Thr
NM_003482.3:c.16001A>C	NP_003473.3:p.Asn5334Thr
XM_005269162.3:c.16001A>C	XP_005269219.1:p.Asn5334Thr
XM_006719614.2:c.16010A>C	XP_006719677.1:p.Asn5337Thr
XM_006719616.2:c.15998A>C	XP_006719679.1:p.Asn5333Thr
XM_011538770.1:c.16010A>C	XP_011537072.1:p.Asn5337Thr
XM_011538771.1:c.16007A>C	XP_011537073.1:p.Asn5336Thr
XM_011538772.1:c.16001A>C	XP_011537074.1:p.Asn5334Thr
XM_011538773.1:c.15998A>C	XP_011537075.1:p.Asn5333Thr
XM_011538774.1:c.15989A>C	XP_011537076.1:p.Asn5330Thr
XM_011538775.1:c.15944A>C	XP_011537077.1:p.Asn5315Thr
XM_011538776.1:c.15917A>C	XP_011537078.1:p.Asn5306Thr
XM_005269162.4:c.16001A>C	XP_005269219.1:p.Asn5334Thr
XM_006719614.4:c.16010A>C	XP_006719677.1:p.Asn5337Thr
XM_006719616.3:c.15998A>C	XP_006719679.1:p.Asn5333Thr
XM_011538770.2:c.16010A>C	XP_011537072.1:p.Asn5337Thr
XM_011538771.2:c.16007A>C	XP_011537073.1:p.Asn5336Thr
XM_011538772.2:c.16001A>C	XP_011537074.1:p.Asn5334Thr
XM_011538773.2:c.15998A>C	XP_011537075.1:p.Asn5333Thr
XM_011538774.2:c.15989A>C	XP_011537076.1:p.Asn5330Thr
XM_011538776.2:c.15917A>C	XP_011537078.1:p.Asn5306Thr
XR_001748874.1:n.16178A>C
NM_003482.4:c.16001A>C MANE Select	NP_003473.3:p.Asn5334Thr