Canonical Allele Identifier: CA384681596

Gene: KMT2D

Linked Data

• MyVariant Identifiers: chr12:g.49418433A>G (hg19) ; chr12:g.49024650A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.49024650A>G , CM000674.2:g.49024650A>G	GRCh38
NC_000012.11:g.49418433A>G , CM000674.1:g.49418433A>G	GRCh37
NC_000012.10:g.47704700A>G	NCBI36
NG_027827.1:g.35675T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000681974.1:n.652T>C
ENST00000683543.2:c.15980T>C	ENSP00000506726.1:p.Met5327Thr
ENST00000683863.1:n.1695T>C
ENST00000684428.1:c.515T>C	ENSP00000507433.1:p.Met172Thr
ENST00000684755.1:n.515T>C
ENST00000685024.1:c.1134T>C
ENST00000685166.1:c.15989T>C	ENSP00000509386.1:p.Met5330Thr
ENST00000688411.1:c.457T>C	ENSP00000510146.1:n.457T>C
ENST00000691932.1:c.59T>C	ENSP00000509037.1:p.Met20Thr
ENST00000692637.1:c.15977T>C	ENSP00000509666.1:p.Met5326Thr
ENST00000301067.12:c.15980T>C MANE Select	ENSP00000301067.7:p.Met5327Thr
ENST00000301067.11:c.15980T>C	ENSP00000301067.7:p.Met5327Thr
NM_003482.3:c.15980T>C	NP_003473.3:p.Met5327Thr
XM_005269162.3:c.15980T>C	XP_005269219.1:p.Met5327Thr
XM_006719614.2:c.15989T>C	XP_006719677.1:p.Met5330Thr
XM_006719616.2:c.15977T>C	XP_006719679.1:p.Met5326Thr
XM_011538770.1:c.15989T>C	XP_011537072.1:p.Met5330Thr
XM_011538771.1:c.15986T>C	XP_011537073.1:p.Met5329Thr
XM_011538772.1:c.15980T>C	XP_011537074.1:p.Met5327Thr
XM_011538773.1:c.15977T>C	XP_011537075.1:p.Met5326Thr
XM_011538774.1:c.15968T>C	XP_011537076.1:p.Met5323Thr
XM_011538775.1:c.15923T>C	XP_011537077.1:p.Met5308Thr
XM_011538776.1:c.15896T>C	XP_011537078.1:p.Met5299Thr
XM_005269162.4:c.15980T>C	XP_005269219.1:p.Met5327Thr
XM_006719614.4:c.15989T>C	XP_006719677.1:p.Met5330Thr
XM_006719616.3:c.15977T>C	XP_006719679.1:p.Met5326Thr
XM_011538770.2:c.15989T>C	XP_011537072.1:p.Met5330Thr
XM_011538771.2:c.15986T>C	XP_011537073.1:p.Met5329Thr
XM_011538772.2:c.15980T>C	XP_011537074.1:p.Met5327Thr
XM_011538773.2:c.15977T>C	XP_011537075.1:p.Met5326Thr
XM_011538774.2:c.15968T>C	XP_011537076.1:p.Met5323Thr
XM_011538776.2:c.15896T>C	XP_011537078.1:p.Met5299Thr
XR_001748874.1:n.16157T>C
NM_003482.4:c.15980T>C MANE Select	NP_003473.3:p.Met5327Thr