Canonical Allele Identifier: CA384626658

Gene: KMT2D

Linked Data

• gnomAD v3: 12-49042101-G-A
• gnomAD v4: 12-49042101-G-A
• MyVariant Identifiers: chr12:g.49435884G>A (hg19) ; chr12:g.49042101G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.49042101G>A , CM000674.2:g.49042101G>A	GRCh38
NC_000012.11:g.49435884G>A , CM000674.1:g.49435884G>A	GRCh37
NC_000012.10:g.47722151G>A	NCBI36
NG_027827.1:g.18224C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650290.2:c.888C>T
ENST00000683543.2:c.6097C>T	ENSP00000506726.1:p.Gln2033Ter
ENST00000685166.1:c.6106C>T	ENSP00000509386.1:p.Gln2036Ter
ENST00000689060.1:c.209C>T
ENST00000689944.1:c.209C>T
ENST00000692637.1:c.6094C>T	ENSP00000509666.1:p.Gln2032Ter
ENST00000301067.12:c.6097C>T MANE Select	ENSP00000301067.7:p.Gln2033Ter
ENST00000301067.11:c.6097C>T	ENSP00000301067.7:p.Gln2033Ter
NM_003482.3:c.6097C>T	NP_003473.3:p.Gln2033Ter
XM_005269162.3:c.6097C>T	XP_005269219.1:p.Gln2033Ter
XM_006719614.2:c.6106C>T	XP_006719677.1:p.Gln2036Ter
XM_006719616.2:c.6094C>T	XP_006719679.1:p.Gln2032Ter
XM_011538770.1:c.6106C>T	XP_011537072.1:p.Gln2036Ter
XM_011538771.1:c.6103C>T	XP_011537073.1:p.Gln2035Ter
XM_011538772.1:c.6097C>T	XP_011537074.1:p.Gln2033Ter
XM_011538773.1:c.6094C>T	XP_011537075.1:p.Gln2032Ter
XM_011538774.1:c.6085C>T	XP_011537076.1:p.Gln2029Ter
XM_011538775.1:c.6106C>T	XP_011537077.1:p.Gln2036Ter
XM_011538776.1:c.6106C>T	XP_011537078.1:p.Gln2036Ter
XR_944740.1:n.8426C>T
XM_005269162.4:c.6097C>T	XP_005269219.1:p.Gln2033Ter
XM_006719614.4:c.6106C>T	XP_006719677.1:p.Gln2036Ter
XM_006719616.3:c.6094C>T	XP_006719679.1:p.Gln2032Ter
XM_011538770.2:c.6106C>T	XP_011537072.1:p.Gln2036Ter
XM_011538771.2:c.6103C>T	XP_011537073.1:p.Gln2035Ter
XM_011538772.2:c.6097C>T	XP_011537074.1:p.Gln2033Ter
XM_011538773.2:c.6094C>T	XP_011537075.1:p.Gln2032Ter
XM_011538774.2:c.6085C>T	XP_011537076.1:p.Gln2029Ter
XM_011538776.2:c.6106C>T	XP_011537078.1:p.Gln2036Ter
XR_001748874.1:n.7415C>T
NM_003482.4:c.6097C>T MANE Select	NP_003473.3:p.Gln2033Ter