Canonical Allele Identifier: CA2034946022

Gene: KMT2D

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.49031923G= , CM000674.2:g.49031923G=	GRCh38
NC_000012.11:g.49425706G= , CM000674.1:g.49425706G=	GRCh37
NC_000012.10:g.47711973G=	NCBI36
NG_027827.1:g.28402C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683543.2:c.12782C=	ENSP00000506726.1:p.Pro4261=
ENST00000685166.1:c.12791C=	ENSP00000509386.1:p.Pro4264=
ENST00000685554.1:c.1752+590C=	ENSP00000508640.1:n.1752+590C=
ENST00000692637.1:c.12779C=	ENSP00000509666.1:p.Pro4260=
ENST00000692841.1:c.4261C=	ENSP00000508711.1:n.4261C=
ENST00000301067.12:c.12782C= MANE Select	ENSP00000301067.7:p.Pro4261=
ENST00000301067.11:c.12782C=	ENSP00000301067.7:p.Pro4261=
NM_003482.3:c.12782C=	NP_003473.3:p.Pro4261=
XM_005269162.3:c.12782C=	XP_005269219.1:p.Pro4261=
XM_006719614.2:c.12791C=	XP_006719677.1:p.Pro4264=
XM_006719616.2:c.12779C=	XP_006719679.1:p.Pro4260=
XM_011538770.1:c.12791C=	XP_011537072.1:p.Pro4264=
XM_011538771.1:c.12788C=	XP_011537073.1:p.Pro4263=
XM_011538772.1:c.12782C=	XP_011537074.1:p.Pro4261=
XM_011538773.1:c.12779C=	XP_011537075.1:p.Pro4260=
XM_011538774.1:c.12770C=	XP_011537076.1:p.Pro4257=
XM_011538775.1:c.12791C=	XP_011537077.1:p.Pro4264=
XM_011538776.1:c.12698C=	XP_011537078.1:p.Pro4233=
XR_944740.1:n.15111C=
XM_005269162.4:c.12782C=	XP_005269219.1:p.Pro4261=
XM_006719614.4:c.12791C=	XP_006719677.1:p.Pro4264=
XM_006719616.3:c.12779C=	XP_006719679.1:p.Pro4260=
XM_011538770.2:c.12791C=	XP_011537072.1:p.Pro4264=
XM_011538771.2:c.12788C=	XP_011537073.1:p.Pro4263=
XM_011538772.2:c.12782C=	XP_011537074.1:p.Pro4261=
XM_011538773.2:c.12779C=	XP_011537075.1:p.Pro4260=
XM_011538774.2:c.12770C=	XP_011537076.1:p.Pro4257=
XM_011538776.2:c.12698C=	XP_011537078.1:p.Pro4233=
XR_001748874.1:n.14100C=
NM_003482.4:c.12782C= MANE Select	NP_003473.3:p.Pro4261=