Canonical Allele Identifier: CA645565081

Gene: KMT2C

Linked Data

• COSMIC: COSM166115 ; COSM166116

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.152148880dup , CM000669.2:g.152148880dup	GRCh38
NC_000007.13:g.151845965dup , CM000669.1:g.151845965dup	GRCh37
NC_000007.12:g.151476898dup	NCBI36
NG_033948.1:g.292126dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682040.1:c.1235dup
ENST00000682116.1:n.2179dup
ENST00000682283.1:c.13218dup	ENSP00000507485.1:p.Lys4407Ter
ENST00000682629.1:n.2347dup
ENST00000683120.1:n.8239dup
ENST00000683178.1:c.3620dup
ENST00000683200.1:c.10557dup	ENSP00000508052.1:p.Lys3520Ter
ENST00000683337.1:n.4677dup
ENST00000683502.1:c.3692dup
ENST00000683621.1:n.1813dup
ENST00000683640.1:n.1763dup
ENST00000684069.1:c.1464dup	ENSP00000507650.1:p.Lys489Ter
ENST00000684261.1:c.7944dup	ENSP00000508097.1:p.Lys2649Ter
ENST00000684649.1:c.3692dup
ENST00000262189.11:c.13047dup MANE Select	ENSP00000262189.6:p.Lys4350Ter
ENST00000360104.8:c.8834dup
ENST00000418061.2:c.3689dup
ENST00000424877.6:c.3623dup
ENST00000679393.1:n.7758dup
ENST00000679560.1:c.7947dup	ENSP00000505094.1:p.Lys2650Ter
ENST00000679882.1:c.12612dup	ENSP00000506154.1:p.Lys4205Ter
ENST00000680029.1:c.3624dup
ENST00000680877.1:c.7947dup	ENSP00000505724.1:p.Lys2650Ter
ENST00000681923.1:n.2062dup
ENST00000262189.10:c.13047dup	ENSP00000262189.6:p.Lys4350Ter
ENST00000355193.6:c.13047dup	ENSP00000347325.3:p.Lys4350Ter
ENST00000360104.7:c.5728dup
ENST00000424877.5:c.2898dup	ENSP00000410411.1:p.Lys967Ter
ENST00000473186.5:n.10929dup
ENST00000558084.5:c.*10567dup	ENSP00000453752.1:n.*10567dup
NM_170606.2:c.13047dup	NP_733751.2:p.Lys4350Ter
XM_005250025.3:c.13263dup	XP_005250082.1:p.Lys4422Ter
XM_005250026.2:c.13260dup	XP_005250083.1:p.Lys4421Ter
XM_005250027.3:c.13260dup	XP_005250084.1:p.Lys4421Ter
XM_005250028.3:c.13263dup	XP_005250085.1:p.Lys4422Ter
XM_005250031.3:c.13098dup	XP_005250088.1:p.Lys4367Ter
XM_006716077.2:c.13260dup	XP_006716140.1:p.Lys4421Ter
XM_006716078.2:c.13191dup	XP_006716141.1:p.Lys4398Ter
XM_006716079.2:c.13095dup	XP_006716142.1:p.Lys4366Ter
XM_011516450.1:c.13215dup	XP_011514752.1:p.Lys4406Ter
XM_011516451.1:c.13143dup	XP_011514753.1:p.Lys4382Ter
XM_011516452.1:c.13110dup	XP_011514754.1:p.Lys4371Ter
XM_011516453.1:c.13026dup	XP_011514755.1:p.Lys4343Ter
XM_011516454.1:c.12348dup	XP_011514756.1:p.Lys4117Ter
XM_011516455.1:c.10809dup	XP_011514757.1:p.Lys3604Ter
XM_011516456.1:c.13215dup	XP_011514758.1:p.Lys4406Ter
XM_005250025.4:c.13263dup	XP_005250082.1:p.Lys4422Ter
XM_005250026.3:c.13260dup	XP_005250083.1:p.Lys4421Ter
XM_005250027.4:c.13260dup	XP_005250084.1:p.Lys4421Ter
XM_005250028.4:c.13263dup	XP_005250085.1:p.Lys4422Ter
XM_005250031.4:c.13098dup	XP_005250088.1:p.Lys4367Ter
XM_006716077.3:c.13260dup	XP_006716140.1:p.Lys4421Ter
XM_006716078.3:c.13191dup	XP_006716141.1:p.Lys4398Ter
XM_006716079.3:c.13095dup	XP_006716142.1:p.Lys4366Ter
XM_011516450.2:c.13215dup	XP_011514752.1:p.Lys4406Ter
XM_011516451.2:c.13143dup	XP_011514753.1:p.Lys4382Ter
XM_011516452.2:c.13110dup	XP_011514754.1:p.Lys4371Ter
XM_011516453.2:c.13026dup	XP_011514755.1:p.Lys4343Ter
XM_011516454.2:c.12348dup	XP_011514756.1:p.Lys4117Ter
XM_011516456.2:c.13215dup	XP_011514758.1:p.Lys4406Ter
XM_017012480.1:c.13263dup	XP_016867969.1:p.Lys4422Ter
XM_017012481.1:c.13260dup	XP_016867970.1:p.Lys4421Ter
XM_017012482.1:c.13260dup	XP_016867971.1:p.Lys4421Ter
XM_017012483.1:c.13260dup	XP_016867972.1:p.Lys4421Ter
XM_017012484.1:c.13230dup	XP_016867973.1:p.Lys4411Ter
XM_017012485.1:c.13212dup	XP_016867974.1:p.Lys4405Ter
XM_017012486.1:c.13188dup	XP_016867975.1:p.Lys4397Ter
XM_017012487.1:c.13116dup	XP_016867976.1:p.Lys4373Ter
XM_017012488.1:c.13080dup	XP_016867977.1:p.Lys4361Ter
XM_017012489.1:c.9933dup	XP_016867978.1:p.Lys3312Ter
XM_017012490.2:c.9537dup	XP_016867979.1:p.Lys3180Ter
XM_024446852.1:c.13260dup	XP_024302620.1:p.Lys4421Ter
XM_024446853.1:c.13188dup	XP_024302621.1:p.Lys4397Ter
NM_170606.3:c.13047dup MANE Select	NP_733751.2:p.Lys4350Ter