Canonical Allele Identifier: CA1752986447
Gene: KMT2C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152148853C= , CM000669.2:g.152148853C= GRCh38
NC_000007.13:g.151845938C= , CM000669.1:g.151845938C= GRCh37
NC_000007.12:g.151476871C= NCBI36
NG_033948.1:g.292153G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682040.1:c.1262G=
ENST00000682116.1:n.2206G=
ENST00000682283.1:c.13245G= ENSP00000507485.1:p.Lys4415=
ENST00000682629.1:n.2374G=
ENST00000683120.1:n.8266G=
ENST00000683178.1:c.3647G=
ENST00000683200.1:c.10584G= ENSP00000508052.1:p.Lys3528=
ENST00000683337.1:n.4704G=
ENST00000683502.1:c.3719G=
ENST00000683621.1:n.1840G=
ENST00000683640.1:n.1790G=
ENST00000684069.1:c.1491G= ENSP00000507650.1:p.Lys497=
ENST00000684261.1:c.7971G= ENSP00000508097.1:p.Lys2657=
ENST00000684649.1:c.3719G=
ENST00000262189.11:c.13074G= MANE Select ENSP00000262189.6:p.Lys4358=
ENST00000360104.8:c.8861G=
ENST00000418061.2:c.3716G=
ENST00000424877.6:c.3650G=
ENST00000679393.1:n.7785G=
ENST00000679560.1:c.7974G= ENSP00000505094.1:p.Lys2658=
ENST00000679882.1:c.12639G= ENSP00000506154.1:p.Lys4213=
ENST00000680029.1:c.3651G=
ENST00000680877.1:c.7974G= ENSP00000505724.1:p.Lys2658=
ENST00000681923.1:n.2089G=
ENST00000262189.10:c.13074G= ENSP00000262189.6:p.Lys4358=
ENST00000355193.6:c.13074G= ENSP00000347325.3:p.Lys4358=
ENST00000360104.7:c.5755G=
ENST00000424877.5:c.2925G= ENSP00000410411.1:p.Lys975=
ENST00000473186.5:n.10956G=
ENST00000558084.5:c.*10594G= ENSP00000453752.1:n.*10594G=
NM_170606.2:c.13074G= NP_733751.2:p.Lys4358=
XM_005250025.3:c.13290G= XP_005250082.1:p.Lys4430=
XM_005250026.2:c.13287G= XP_005250083.1:p.Lys4429=
XM_005250027.3:c.13287G= XP_005250084.1:p.Lys4429=
XM_005250028.3:c.13290G= XP_005250085.1:p.Lys4430=
XM_005250031.3:c.13125G= XP_005250088.1:p.Lys4375=
XM_006716077.2:c.13287G= XP_006716140.1:p.Lys4429=
XM_006716078.2:c.13218G= XP_006716141.1:p.Lys4406=
XM_006716079.2:c.13122G= XP_006716142.1:p.Lys4374=
XM_011516450.1:c.13242G= XP_011514752.1:p.Lys4414=
XM_011516451.1:c.13170G= XP_011514753.1:p.Lys4390=
XM_011516452.1:c.13137G= XP_011514754.1:p.Lys4379=
XM_011516453.1:c.13053G= XP_011514755.1:p.Lys4351=
XM_011516454.1:c.12375G= XP_011514756.1:p.Lys4125=
XM_011516455.1:c.10836G= XP_011514757.1:p.Lys3612=
XM_011516456.1:c.13242G= XP_011514758.1:p.Lys4414=
XM_005250025.4:c.13290G= XP_005250082.1:p.Lys4430=
XM_005250026.3:c.13287G= XP_005250083.1:p.Lys4429=
XM_005250027.4:c.13287G= XP_005250084.1:p.Lys4429=
XM_005250028.4:c.13290G= XP_005250085.1:p.Lys4430=
XM_005250031.4:c.13125G= XP_005250088.1:p.Lys4375=
XM_006716077.3:c.13287G= XP_006716140.1:p.Lys4429=
XM_006716078.3:c.13218G= XP_006716141.1:p.Lys4406=
XM_006716079.3:c.13122G= XP_006716142.1:p.Lys4374=
XM_011516450.2:c.13242G= XP_011514752.1:p.Lys4414=
XM_011516451.2:c.13170G= XP_011514753.1:p.Lys4390=
XM_011516452.2:c.13137G= XP_011514754.1:p.Lys4379=
XM_011516453.2:c.13053G= XP_011514755.1:p.Lys4351=
XM_011516454.2:c.12375G= XP_011514756.1:p.Lys4125=
XM_011516456.2:c.13242G= XP_011514758.1:p.Lys4414=
XM_017012480.1:c.13290G= XP_016867969.1:p.Lys4430=
XM_017012481.1:c.13287G= XP_016867970.1:p.Lys4429=
XM_017012482.1:c.13287G= XP_016867971.1:p.Lys4429=
XM_017012483.1:c.13287G= XP_016867972.1:p.Lys4429=
XM_017012484.1:c.13257G= XP_016867973.1:p.Lys4419=
XM_017012485.1:c.13239G= XP_016867974.1:p.Lys4413=
XM_017012486.1:c.13215G= XP_016867975.1:p.Lys4405=
XM_017012487.1:c.13143G= XP_016867976.1:p.Lys4381=
XM_017012488.1:c.13107G= XP_016867977.1:p.Lys4369=
XM_017012489.1:c.9960G= XP_016867978.1:p.Lys3320=
XM_017012490.2:c.9564G= XP_016867979.1:p.Lys3188=
XM_024446852.1:c.13287G= XP_024302620.1:p.Lys4429=
XM_024446853.1:c.13215G= XP_024302621.1:p.Lys4405=
NM_170606.3:c.13074G= MANE Select NP_733751.2:p.Lys4358=