Canonical Allele Identifier: CA384703319

Gene: KMT2D

Linked Data

• dbSNP Id: rs772023360
• MyVariant Identifiers: chr12:g.49424720C>G (hg19) ; chr12:g.49030937C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.49030937C>G , CM000674.2:g.49030937C>G	GRCh38
NC_000012.11:g.49424720C>G , CM000674.1:g.49424720C>G	GRCh37
NC_000012.10:g.47710987C>G	NCBI36
NG_027827.1:g.29388G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000552391.2:n.327G>C
ENST00000683543.2:c.13627G>C	ENSP00000506726.1:p.Asp4543His
ENST00000685166.1:c.13636G>C	ENSP00000509386.1:p.Asp4546His
ENST00000685982.1:c.139-169G>C	ENSP00000508613.1:n.139-169G>C
ENST00000691986.1:c.138+238G>C	ENSP00000509196.1:n.138+238G>C
ENST00000692637.1:c.13624G>C	ENSP00000509666.1:p.Asp4542His
ENST00000692973.1:c.228G>C	ENSP00000508893.1:n.228G>C
ENST00000301067.12:c.13627G>C MANE Select	ENSP00000301067.7:p.Asp4543His
ENST00000301067.11:c.13627G>C	ENSP00000301067.7:p.Asp4543His
ENST00000552391.1:n.327G>C
NM_003482.3:c.13627G>C	NP_003473.3:p.Asp4543His
XM_005269162.3:c.13627G>C	XP_005269219.1:p.Asp4543His
XM_006719614.2:c.13636G>C	XP_006719677.1:p.Asp4546His
XM_006719616.2:c.13624G>C	XP_006719679.1:p.Asp4542His
XM_011538770.1:c.13636G>C	XP_011537072.1:p.Asp4546His
XM_011538771.1:c.13633G>C	XP_011537073.1:p.Asp4545His
XM_011538772.1:c.13627G>C	XP_011537074.1:p.Asp4543His
XM_011538773.1:c.13624G>C	XP_011537075.1:p.Asp4542His
XM_011538774.1:c.13615G>C	XP_011537076.1:p.Asp4539His
XM_011538775.1:c.13636G>C	XP_011537077.1:p.Asp4546His
XM_011538776.1:c.13543G>C	XP_011537078.1:p.Asp4515His
XR_944740.1:n.15956G>C
XM_005269162.4:c.13627G>C	XP_005269219.1:p.Asp4543His
XM_006719614.4:c.13636G>C	XP_006719677.1:p.Asp4546His
XM_006719616.3:c.13624G>C	XP_006719679.1:p.Asp4542His
XM_011538770.2:c.13636G>C	XP_011537072.1:p.Asp4546His
XM_011538771.2:c.13633G>C	XP_011537073.1:p.Asp4545His
XM_011538772.2:c.13627G>C	XP_011537074.1:p.Asp4543His
XM_011538773.2:c.13624G>C	XP_011537075.1:p.Asp4542His
XM_011538774.2:c.13615G>C	XP_011537076.1:p.Asp4539His
XM_011538776.2:c.13543G>C	XP_011537078.1:p.Asp4515His
XR_001748874.1:n.14945G>C
NM_003482.4:c.13627G>C MANE Select	NP_003473.3:p.Asp4543His