Canonical Allele Identifier: CA370093070

Gene: KMT2C

Linked Data

• MyVariant Identifiers: chr7:g.151845879T>A (hg19) ; chr7:g.152148794T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.152148794T>A , CM000669.2:g.152148794T>A	GRCh38
NC_000007.13:g.151845879T>A , CM000669.1:g.151845879T>A	GRCh37
NC_000007.12:g.151476812T>A	NCBI36
NG_033948.1:g.292212A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682040.1:c.1321A>T
ENST00000682116.1:n.2265A>T
ENST00000682283.1:c.13304A>T	ENSP00000507485.1:p.Glu4435Val
ENST00000682629.1:n.2433A>T
ENST00000683120.1:n.8325A>T
ENST00000683178.1:c.3706A>T
ENST00000683200.1:c.10643A>T	ENSP00000508052.1:p.Glu3548Val
ENST00000683337.1:n.4763A>T
ENST00000683502.1:c.3778A>T
ENST00000683621.1:n.1899A>T
ENST00000683640.1:n.1849A>T
ENST00000684069.1:c.1550A>T	ENSP00000507650.1:p.Glu517Val
ENST00000684261.1:c.8030A>T	ENSP00000508097.1:p.Glu2677Val
ENST00000684649.1:c.3778A>T
ENST00000262189.11:c.13133A>T MANE Select	ENSP00000262189.6:p.Glu4378Val
ENST00000360104.8:c.8920A>T
ENST00000418061.2:c.3775A>T
ENST00000424877.6:c.3709A>T
ENST00000679393.1:n.7844A>T
ENST00000679560.1:c.8033A>T	ENSP00000505094.1:p.Glu2678Val
ENST00000679882.1:c.12698A>T	ENSP00000506154.1:p.Glu4233Val
ENST00000680029.1:c.3710A>T
ENST00000680877.1:c.8033A>T	ENSP00000505724.1:p.Glu2678Val
ENST00000681923.1:n.2148A>T
ENST00000262189.10:c.13133A>T	ENSP00000262189.6:p.Glu4378Val
ENST00000355193.6:c.13133A>T	ENSP00000347325.3:p.Glu4378Val
ENST00000360104.7:c.5814A>T
ENST00000424877.5:c.2984A>T	ENSP00000410411.1:p.Glu995Val
ENST00000473186.5:n.11015A>T
ENST00000558084.5:c.*10653A>T	ENSP00000453752.1:n.*10653A>T
NM_170606.2:c.13133A>T	NP_733751.2:p.Glu4378Val
XM_005250025.3:c.13349A>T	XP_005250082.1:p.Glu4450Val
XM_005250026.2:c.13346A>T	XP_005250083.1:p.Glu4449Val
XM_005250027.3:c.13346A>T	XP_005250084.1:p.Glu4449Val
XM_005250028.3:c.13349A>T	XP_005250085.1:p.Glu4450Val
XM_005250031.3:c.13184A>T	XP_005250088.1:p.Glu4395Val
XM_006716077.2:c.13346A>T	XP_006716140.1:p.Glu4449Val
XM_006716078.2:c.13277A>T	XP_006716141.1:p.Glu4426Val
XM_006716079.2:c.13181A>T	XP_006716142.1:p.Glu4394Val
XM_011516450.1:c.13301A>T	XP_011514752.1:p.Glu4434Val
XM_011516451.1:c.13229A>T	XP_011514753.1:p.Glu4410Val
XM_011516452.1:c.13196A>T	XP_011514754.1:p.Glu4399Val
XM_011516453.1:c.13112A>T	XP_011514755.1:p.Glu4371Val
XM_011516454.1:c.12434A>T	XP_011514756.1:p.Glu4145Val
XM_011516455.1:c.10895A>T	XP_011514757.1:p.Glu3632Val
XM_011516456.1:c.13301A>T	XP_011514758.1:p.Glu4434Val
XM_005250025.4:c.13349A>T	XP_005250082.1:p.Glu4450Val
XM_005250026.3:c.13346A>T	XP_005250083.1:p.Glu4449Val
XM_005250027.4:c.13346A>T	XP_005250084.1:p.Glu4449Val
XM_005250028.4:c.13349A>T	XP_005250085.1:p.Glu4450Val
XM_005250031.4:c.13184A>T	XP_005250088.1:p.Glu4395Val
XM_006716077.3:c.13346A>T	XP_006716140.1:p.Glu4449Val
XM_006716078.3:c.13277A>T	XP_006716141.1:p.Glu4426Val
XM_006716079.3:c.13181A>T	XP_006716142.1:p.Glu4394Val
XM_011516450.2:c.13301A>T	XP_011514752.1:p.Glu4434Val
XM_011516451.2:c.13229A>T	XP_011514753.1:p.Glu4410Val
XM_011516452.2:c.13196A>T	XP_011514754.1:p.Glu4399Val
XM_011516453.2:c.13112A>T	XP_011514755.1:p.Glu4371Val
XM_011516454.2:c.12434A>T	XP_011514756.1:p.Glu4145Val
XM_011516456.2:c.13301A>T	XP_011514758.1:p.Glu4434Val
XM_017012480.1:c.13349A>T	XP_016867969.1:p.Glu4450Val
XM_017012481.1:c.13346A>T	XP_016867970.1:p.Glu4449Val
XM_017012482.1:c.13346A>T	XP_016867971.1:p.Glu4449Val
XM_017012483.1:c.13346A>T	XP_016867972.1:p.Glu4449Val
XM_017012484.1:c.13316A>T	XP_016867973.1:p.Glu4439Val
XM_017012485.1:c.13298A>T	XP_016867974.1:p.Glu4433Val
XM_017012486.1:c.13274A>T	XP_016867975.1:p.Glu4425Val
XM_017012487.1:c.13202A>T	XP_016867976.1:p.Glu4401Val
XM_017012488.1:c.13166A>T	XP_016867977.1:p.Glu4389Val
XM_017012489.1:c.10019A>T	XP_016867978.1:p.Glu3340Val
XM_017012490.2:c.9623A>T	XP_016867979.1:p.Glu3208Val
XM_024446852.1:c.13346A>T	XP_024302620.1:p.Glu4449Val
XM_024446853.1:c.13274A>T	XP_024302621.1:p.Glu4425Val
NM_170606.3:c.13133A>T MANE Select	NP_733751.2:p.Glu4378Val