Canonical Allele Identifier: CA384677394

Gene: KMT2D

Linked Data

• dbSNP Id: rs2137706198
• MyVariant Identifiers: chr12:g.49416383T>G (hg19) ; chr12:g.49022600T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.49022600T>G , CM000674.2:g.49022600T>G	GRCh38
NC_000012.11:g.49416383T>G , CM000674.1:g.49416383T>G	GRCh37
NC_000012.10:g.47702650T>G	NCBI36
NG_027827.1:g.37725A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000526209.2:c.298A>C
ENST00000681974.1:n.1000A>C
ENST00000682693.1:n.1962A>C
ENST00000682886.1:n.498A>C
ENST00000683543.2:c.16376A>C	ENSP00000506726.1:p.Tyr5459Ser
ENST00000683988.1:c.299A>C	ENSP00000506939.1:p.Tyr100Ser
ENST00000684428.1:c.863A>C	ENSP00000507433.1:p.Tyr288Ser
ENST00000684755.1:n.911A>C
ENST00000685024.1:c.1482A>C
ENST00000685166.1:c.16337A>C	ENSP00000509386.1:p.Tyr5446Ser
ENST00000688411.1:c.805A>C	ENSP00000510146.1:n.805A>C
ENST00000691932.1:c.329A>C	ENSP00000509037.1:p.Tyr110Ser
ENST00000692637.1:c.16325A>C	ENSP00000509666.1:p.Tyr5442Ser
ENST00000301067.12:c.16328A>C MANE Select	ENSP00000301067.7:p.Tyr5443Ser
ENST00000301067.11:c.16328A>C	ENSP00000301067.7:p.Tyr5443Ser
ENST00000526209.1:c.371A>C	ENSP00000435714.1:p.Tyr124Ser
NM_003482.3:c.16328A>C	NP_003473.3:p.Tyr5443Ser
XM_005269162.3:c.16328A>C	XP_005269219.1:p.Tyr5443Ser
XM_006719614.2:c.16337A>C	XP_006719677.1:p.Tyr5446Ser
XM_006719616.2:c.16325A>C	XP_006719679.1:p.Tyr5442Ser
XM_011538770.1:c.16385A>C	XP_011537072.1:p.Tyr5462Ser
XM_011538771.1:c.16382A>C	XP_011537073.1:p.Tyr5461Ser
XM_011538772.1:c.16376A>C	XP_011537074.1:p.Tyr5459Ser
XM_011538773.1:c.16373A>C	XP_011537075.1:p.Tyr5458Ser
XM_011538774.1:c.16364A>C	XP_011537076.1:p.Tyr5455Ser
XM_011538775.1:c.16319A>C	XP_011537077.1:p.Tyr5440Ser
XM_011538776.1:c.16292A>C	XP_011537078.1:p.Tyr5431Ser
XM_005269162.4:c.16328A>C	XP_005269219.1:p.Tyr5443Ser
XM_006719614.4:c.16337A>C	XP_006719677.1:p.Tyr5446Ser
XM_006719616.3:c.16325A>C	XP_006719679.1:p.Tyr5442Ser
XM_011538770.2:c.16385A>C	XP_011537072.1:p.Tyr5462Ser
XM_011538771.2:c.16382A>C	XP_011537073.1:p.Tyr5461Ser
XM_011538772.2:c.16376A>C	XP_011537074.1:p.Tyr5459Ser
XM_011538773.2:c.16373A>C	XP_011537075.1:p.Tyr5458Ser
XM_011538774.2:c.16364A>C	XP_011537076.1:p.Tyr5455Ser
XM_011538776.2:c.16292A>C	XP_011537078.1:p.Tyr5431Ser
XR_001748874.1:n.16505A>C
NM_003482.4:c.16328A>C MANE Select	NP_003473.3:p.Tyr5443Ser