Canonical Allele Identifier: CA384676534

Gene: KMT2D

Linked Data

• dbSNP Id: rs759195065
• MyVariant Identifiers: chr12:g.49415930T>A (hg19) ; chr12:g.49022147T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.49022147T>A , CM000674.2:g.49022147T>A	GRCh38
NC_000012.11:g.49415930T>A , CM000674.1:g.49415930T>A	GRCh37
NC_000012.10:g.47702197T>A	NCBI36
NG_027827.1:g.38178A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000526209.2:c.387A>T
ENST00000681974.1:n.1089A>T
ENST00000682693.1:n.2051A>T
ENST00000682886.1:n.823A>T
ENST00000683543.2:c.16465A>T	ENSP00000506726.1:p.Ile5489Phe
ENST00000683988.1:c.388A>T	ENSP00000506939.1:p.Ile130Phe
ENST00000684428.1:c.1010A>T	ENSP00000507433.1:n.1010A>T
ENST00000685024.1:c.1571A>T
ENST00000685166.1:c.16426A>T	ENSP00000509386.1:p.Ile5476Phe
ENST00000691932.1:c.418A>T	ENSP00000509037.1:p.Ile140Phe
ENST00000692637.1:c.16414A>T	ENSP00000509666.1:p.Ile5472Phe
ENST00000301067.12:c.16417A>T MANE Select	ENSP00000301067.7:p.Ile5473Phe
ENST00000301067.11:c.16417A>T	ENSP00000301067.7:p.Ile5473Phe
ENST00000526209.1:c.460A>T	ENSP00000435714.1:p.Ile154Phe
NM_003482.3:c.16417A>T	NP_003473.3:p.Ile5473Phe
XM_005269162.3:c.16417A>T	XP_005269219.1:p.Ile5473Phe
XM_006719614.2:c.16426A>T	XP_006719677.1:p.Ile5476Phe
XM_006719616.2:c.16414A>T	XP_006719679.1:p.Ile5472Phe
XM_011538770.1:c.16474A>T	XP_011537072.1:p.Ile5492Phe
XM_011538771.1:c.16471A>T	XP_011537073.1:p.Ile5491Phe
XM_011538772.1:c.16465A>T	XP_011537074.1:p.Ile5489Phe
XM_011538773.1:c.16462A>T	XP_011537075.1:p.Ile5488Phe
XM_011538774.1:c.16453A>T	XP_011537076.1:p.Ile5485Phe
XM_011538775.1:c.16408A>T	XP_011537077.1:p.Ile5470Phe
XM_011538776.1:c.16381A>T	XP_011537078.1:p.Ile5461Phe
XM_005269162.4:c.16417A>T	XP_005269219.1:p.Ile5473Phe
XM_006719614.4:c.16426A>T	XP_006719677.1:p.Ile5476Phe
XM_006719616.3:c.16414A>T	XP_006719679.1:p.Ile5472Phe
XM_011538770.2:c.16474A>T	XP_011537072.1:p.Ile5492Phe
XM_011538771.2:c.16471A>T	XP_011537073.1:p.Ile5491Phe
XM_011538772.2:c.16465A>T	XP_011537074.1:p.Ile5489Phe
XM_011538773.2:c.16462A>T	XP_011537075.1:p.Ile5488Phe
XM_011538774.2:c.16453A>T	XP_011537076.1:p.Ile5485Phe
XM_011538776.2:c.16381A>T	XP_011537078.1:p.Ile5461Phe
XR_001748874.1:n.16594A>T
NM_003482.4:c.16417A>T MANE Select	NP_003473.3:p.Ile5473Phe