Canonical Allele Identifier: CA236638613

Gene: KMT2D

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.49031381C>T , CM000674.2:g.49031381C>T	GRCh38
NC_000012.11:g.49425164C>T , CM000674.1:g.49425164C>T	GRCh37
NC_000012.10:g.47711431C>T	NCBI36
NG_027827.1:g.28944G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_003482.4:c.13324G>A MANE Select	NP_003473.3:p.Ala4442Thr
ENST00000301067.12:c.13324G>A MANE Select	ENSP00000301067.7:p.Ala4442Thr
NM_003482.3:c.13324G>A	NP_003473.3:p.Ala4442Thr
ENST00000301067.11:c.13324G>A	ENSP00000301067.7:p.Ala4442Thr
ENST00000552391.1:n.24G>A
ENST00000552391.2:n.24G>A
ENST00000683543.2:c.13324G>A	ENSP00000506726.1:p.Ala4442Thr
ENST00000685166.1:c.13333G>A	ENSP00000509386.1:p.Ala4445Thr
ENST00000685554.1:c.1753-69G>A	ENSP00000508640.1:n.1753-69G>A
ENST00000692637.1:c.13321G>A	ENSP00000509666.1:p.Ala4441Thr
ENST00000692841.1:c.4803G>A	ENSP00000508711.1:n.4803G>A
XM_005269162.3:c.13324G>A	XP_005269219.1:p.Ala4442Thr
XM_005269162.4:c.13324G>A	XP_005269219.1:p.Ala4442Thr
XM_006719614.2:c.13333G>A	XP_006719677.1:p.Ala4445Thr
XM_006719614.4:c.13333G>A	XP_006719677.1:p.Ala4445Thr
XM_006719616.2:c.13321G>A	XP_006719679.1:p.Ala4441Thr
XM_006719616.3:c.13321G>A	XP_006719679.1:p.Ala4441Thr
XM_011538770.1:c.13333G>A	XP_011537072.1:p.Ala4445Thr
XM_011538770.2:c.13333G>A	XP_011537072.1:p.Ala4445Thr
XM_011538771.1:c.13330G>A	XP_011537073.1:p.Ala4444Thr
XM_011538771.2:c.13330G>A	XP_011537073.1:p.Ala4444Thr
XM_011538772.1:c.13324G>A	XP_011537074.1:p.Ala4442Thr
XM_011538772.2:c.13324G>A	XP_011537074.1:p.Ala4442Thr
XM_011538773.1:c.13321G>A	XP_011537075.1:p.Ala4441Thr
XM_011538773.2:c.13321G>A	XP_011537075.1:p.Ala4441Thr
XM_011538774.1:c.13312G>A	XP_011537076.1:p.Ala4438Thr
XM_011538774.2:c.13312G>A	XP_011537076.1:p.Ala4438Thr
XM_011538775.1:c.13333G>A	XP_011537077.1:p.Ala4445Thr
XM_011538776.1:c.13240G>A	XP_011537078.1:p.Ala4414Thr
XM_011538776.2:c.13240G>A	XP_011537078.1:p.Ala4414Thr
XR_001748874.1:n.14642G>A
XR_944740.1:n.15653G>A