Canonical Allele Identifier: CA1752986482
Gene: KMT2C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152148872C= , CM000669.2:g.152148872C= GRCh38
NC_000007.13:g.151845957C= , CM000669.1:g.151845957C= GRCh37
NC_000007.12:g.151476890C= NCBI36
NG_033948.1:g.292134G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682040.1:c.1243G=
ENST00000682116.1:n.2187G=
ENST00000682283.1:c.13226G= ENSP00000507485.1:p.Trp4409=
ENST00000682629.1:n.2355G=
ENST00000683120.1:n.8247G=
ENST00000683178.1:c.3628G=
ENST00000683200.1:c.10565G= ENSP00000508052.1:p.Trp3522=
ENST00000683337.1:n.4685G=
ENST00000683502.1:c.3700G=
ENST00000683621.1:n.1821G=
ENST00000683640.1:n.1771G=
ENST00000684069.1:c.1472G= ENSP00000507650.1:p.Trp491=
ENST00000684261.1:c.7952G= ENSP00000508097.1:p.Trp2651=
ENST00000684649.1:c.3700G=
ENST00000262189.11:c.13055G= MANE Select ENSP00000262189.6:p.Trp4352=
ENST00000360104.8:c.8842G=
ENST00000418061.2:c.3697G=
ENST00000424877.6:c.3631G=
ENST00000679393.1:n.7766G=
ENST00000679560.1:c.7955G= ENSP00000505094.1:p.Trp2652=
ENST00000679882.1:c.12620G= ENSP00000506154.1:p.Trp4207=
ENST00000680029.1:c.3632G=
ENST00000680877.1:c.7955G= ENSP00000505724.1:p.Trp2652=
ENST00000681923.1:n.2070G=
ENST00000262189.10:c.13055G= ENSP00000262189.6:p.Trp4352=
ENST00000355193.6:c.13055G= ENSP00000347325.3:p.Trp4352=
ENST00000360104.7:c.5736G=
ENST00000424877.5:c.2906G= ENSP00000410411.1:p.Trp969=
ENST00000473186.5:n.10937G=
ENST00000558084.5:c.*10575G= ENSP00000453752.1:n.*10575G=
NM_170606.2:c.13055G= NP_733751.2:p.Trp4352=
XM_005250025.3:c.13271G= XP_005250082.1:p.Trp4424=
XM_005250026.2:c.13268G= XP_005250083.1:p.Trp4423=
XM_005250027.3:c.13268G= XP_005250084.1:p.Trp4423=
XM_005250028.3:c.13271G= XP_005250085.1:p.Trp4424=
XM_005250031.3:c.13106G= XP_005250088.1:p.Trp4369=
XM_006716077.2:c.13268G= XP_006716140.1:p.Trp4423=
XM_006716078.2:c.13199G= XP_006716141.1:p.Trp4400=
XM_006716079.2:c.13103G= XP_006716142.1:p.Trp4368=
XM_011516450.1:c.13223G= XP_011514752.1:p.Trp4408=
XM_011516451.1:c.13151G= XP_011514753.1:p.Trp4384=
XM_011516452.1:c.13118G= XP_011514754.1:p.Trp4373=
XM_011516453.1:c.13034G= XP_011514755.1:p.Trp4345=
XM_011516454.1:c.12356G= XP_011514756.1:p.Trp4119=
XM_011516455.1:c.10817G= XP_011514757.1:p.Trp3606=
XM_011516456.1:c.13223G= XP_011514758.1:p.Trp4408=
XM_005250025.4:c.13271G= XP_005250082.1:p.Trp4424=
XM_005250026.3:c.13268G= XP_005250083.1:p.Trp4423=
XM_005250027.4:c.13268G= XP_005250084.1:p.Trp4423=
XM_005250028.4:c.13271G= XP_005250085.1:p.Trp4424=
XM_005250031.4:c.13106G= XP_005250088.1:p.Trp4369=
XM_006716077.3:c.13268G= XP_006716140.1:p.Trp4423=
XM_006716078.3:c.13199G= XP_006716141.1:p.Trp4400=
XM_006716079.3:c.13103G= XP_006716142.1:p.Trp4368=
XM_011516450.2:c.13223G= XP_011514752.1:p.Trp4408=
XM_011516451.2:c.13151G= XP_011514753.1:p.Trp4384=
XM_011516452.2:c.13118G= XP_011514754.1:p.Trp4373=
XM_011516453.2:c.13034G= XP_011514755.1:p.Trp4345=
XM_011516454.2:c.12356G= XP_011514756.1:p.Trp4119=
XM_011516456.2:c.13223G= XP_011514758.1:p.Trp4408=
XM_017012480.1:c.13271G= XP_016867969.1:p.Trp4424=
XM_017012481.1:c.13268G= XP_016867970.1:p.Trp4423=
XM_017012482.1:c.13268G= XP_016867971.1:p.Trp4423=
XM_017012483.1:c.13268G= XP_016867972.1:p.Trp4423=
XM_017012484.1:c.13238G= XP_016867973.1:p.Trp4413=
XM_017012485.1:c.13220G= XP_016867974.1:p.Trp4407=
XM_017012486.1:c.13196G= XP_016867975.1:p.Trp4399=
XM_017012487.1:c.13124G= XP_016867976.1:p.Trp4375=
XM_017012488.1:c.13088G= XP_016867977.1:p.Trp4363=
XM_017012489.1:c.9941G= XP_016867978.1:p.Trp3314=
XM_017012490.2:c.9545G= XP_016867979.1:p.Trp3182=
XM_024446852.1:c.13268G= XP_024302620.1:p.Trp4423=
XM_024446853.1:c.13196G= XP_024302621.1:p.Trp4399=
NM_170606.3:c.13055G= MANE Select NP_733751.2:p.Trp4352=