Canonical Allele Identifier: CA384717148

Gene: KMT2D

Linked Data

• MyVariant Identifiers: chr12:g.49426867G>T (hg19) ; chr12:g.49033084G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.49033084G>T , CM000674.2:g.49033084G>T	GRCh38
NC_000012.11:g.49426867G>T , CM000674.1:g.49426867G>T	GRCh37
NC_000012.10:g.47713134G>T	NCBI36
NG_027827.1:g.27241C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683543.2:c.11621C>A	ENSP00000506726.1:p.Ser3874Tyr
ENST00000685166.1:c.11630C>A	ENSP00000509386.1:p.Ser3877Tyr
ENST00000685554.1:c.1181C>A	ENSP00000508640.1:p.Ser394Tyr
ENST00000687201.1:c.3200C>A	ENSP00000510037.1:p.Ser1067Tyr
ENST00000692637.1:c.11618C>A	ENSP00000509666.1:p.Ser3873Tyr
ENST00000692841.1:c.3100C>A	ENSP00000508711.1:n.3100C>A
ENST00000301067.12:c.11621C>A MANE Select	ENSP00000301067.7:p.Ser3874Tyr
ENST00000301067.11:c.11621C>A	ENSP00000301067.7:p.Ser3874Tyr
NM_003482.3:c.11621C>A	NP_003473.3:p.Ser3874Tyr
XM_005269162.3:c.11621C>A	XP_005269219.1:p.Ser3874Tyr
XM_006719614.2:c.11630C>A	XP_006719677.1:p.Ser3877Tyr
XM_006719616.2:c.11618C>A	XP_006719679.1:p.Ser3873Tyr
XM_011538770.1:c.11630C>A	XP_011537072.1:p.Ser3877Tyr
XM_011538771.1:c.11627C>A	XP_011537073.1:p.Ser3876Tyr
XM_011538772.1:c.11621C>A	XP_011537074.1:p.Ser3874Tyr
XM_011538773.1:c.11618C>A	XP_011537075.1:p.Ser3873Tyr
XM_011538774.1:c.11609C>A	XP_011537076.1:p.Ser3870Tyr
XM_011538775.1:c.11630C>A	XP_011537077.1:p.Ser3877Tyr
XM_011538776.1:c.11537C>A	XP_011537078.1:p.Ser3846Tyr
XR_944740.1:n.13950C>A
XM_005269162.4:c.11621C>A	XP_005269219.1:p.Ser3874Tyr
XM_006719614.4:c.11630C>A	XP_006719677.1:p.Ser3877Tyr
XM_006719616.3:c.11618C>A	XP_006719679.1:p.Ser3873Tyr
XM_011538770.2:c.11630C>A	XP_011537072.1:p.Ser3877Tyr
XM_011538771.2:c.11627C>A	XP_011537073.1:p.Ser3876Tyr
XM_011538772.2:c.11621C>A	XP_011537074.1:p.Ser3874Tyr
XM_011538773.2:c.11618C>A	XP_011537075.1:p.Ser3873Tyr
XM_011538774.2:c.11609C>A	XP_011537076.1:p.Ser3870Tyr
XM_011538776.2:c.11537C>A	XP_011537078.1:p.Ser3846Tyr
XR_001748874.1:n.12939C>A
NM_003482.4:c.11621C>A MANE Select	NP_003473.3:p.Ser3874Tyr