Canonical Allele Identifier: CA1752986400
Gene: KMT2C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152148818G= , CM000669.2:g.152148818G= GRCh38
NC_000007.13:g.151845903G= , CM000669.1:g.151845903G= GRCh37
NC_000007.12:g.151476836G= NCBI36
NG_033948.1:g.292188C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682040.1:c.1297C=
ENST00000682116.1:n.2241C=
ENST00000682283.1:c.13280C= ENSP00000507485.1:p.Thr4427=
ENST00000682629.1:n.2409C=
ENST00000683120.1:n.8301C=
ENST00000683178.1:c.3682C=
ENST00000683200.1:c.10619C= ENSP00000508052.1:p.Thr3540=
ENST00000683337.1:n.4739C=
ENST00000683502.1:c.3754C=
ENST00000683621.1:n.1875C=
ENST00000683640.1:n.1825C=
ENST00000684069.1:c.1526C= ENSP00000507650.1:p.Thr509=
ENST00000684261.1:c.8006C= ENSP00000508097.1:p.Thr2669=
ENST00000684649.1:c.3754C=
ENST00000262189.11:c.13109C= MANE Select ENSP00000262189.6:p.Thr4370=
ENST00000360104.8:c.8896C=
ENST00000418061.2:c.3751C=
ENST00000424877.6:c.3685C=
ENST00000679393.1:n.7820C=
ENST00000679560.1:c.8009C= ENSP00000505094.1:p.Thr2670=
ENST00000679882.1:c.12674C= ENSP00000506154.1:p.Thr4225=
ENST00000680029.1:c.3686C=
ENST00000680877.1:c.8009C= ENSP00000505724.1:p.Thr2670=
ENST00000681923.1:n.2124C=
ENST00000262189.10:c.13109C= ENSP00000262189.6:p.Thr4370=
ENST00000355193.6:c.13109C= ENSP00000347325.3:p.Thr4370=
ENST00000360104.7:c.5790C=
ENST00000424877.5:c.2960C= ENSP00000410411.1:p.Thr987=
ENST00000473186.5:n.10991C=
ENST00000558084.5:c.*10629C= ENSP00000453752.1:n.*10629C=
NM_170606.2:c.13109C= NP_733751.2:p.Thr4370=
XM_005250025.3:c.13325C= XP_005250082.1:p.Thr4442=
XM_005250026.2:c.13322C= XP_005250083.1:p.Thr4441=
XM_005250027.3:c.13322C= XP_005250084.1:p.Thr4441=
XM_005250028.3:c.13325C= XP_005250085.1:p.Thr4442=
XM_005250031.3:c.13160C= XP_005250088.1:p.Thr4387=
XM_006716077.2:c.13322C= XP_006716140.1:p.Thr4441=
XM_006716078.2:c.13253C= XP_006716141.1:p.Thr4418=
XM_006716079.2:c.13157C= XP_006716142.1:p.Thr4386=
XM_011516450.1:c.13277C= XP_011514752.1:p.Thr4426=
XM_011516451.1:c.13205C= XP_011514753.1:p.Thr4402=
XM_011516452.1:c.13172C= XP_011514754.1:p.Thr4391=
XM_011516453.1:c.13088C= XP_011514755.1:p.Thr4363=
XM_011516454.1:c.12410C= XP_011514756.1:p.Thr4137=
XM_011516455.1:c.10871C= XP_011514757.1:p.Thr3624=
XM_011516456.1:c.13277C= XP_011514758.1:p.Thr4426=
XM_005250025.4:c.13325C= XP_005250082.1:p.Thr4442=
XM_005250026.3:c.13322C= XP_005250083.1:p.Thr4441=
XM_005250027.4:c.13322C= XP_005250084.1:p.Thr4441=
XM_005250028.4:c.13325C= XP_005250085.1:p.Thr4442=
XM_005250031.4:c.13160C= XP_005250088.1:p.Thr4387=
XM_006716077.3:c.13322C= XP_006716140.1:p.Thr4441=
XM_006716078.3:c.13253C= XP_006716141.1:p.Thr4418=
XM_006716079.3:c.13157C= XP_006716142.1:p.Thr4386=
XM_011516450.2:c.13277C= XP_011514752.1:p.Thr4426=
XM_011516451.2:c.13205C= XP_011514753.1:p.Thr4402=
XM_011516452.2:c.13172C= XP_011514754.1:p.Thr4391=
XM_011516453.2:c.13088C= XP_011514755.1:p.Thr4363=
XM_011516454.2:c.12410C= XP_011514756.1:p.Thr4137=
XM_011516456.2:c.13277C= XP_011514758.1:p.Thr4426=
XM_017012480.1:c.13325C= XP_016867969.1:p.Thr4442=
XM_017012481.1:c.13322C= XP_016867970.1:p.Thr4441=
XM_017012482.1:c.13322C= XP_016867971.1:p.Thr4441=
XM_017012483.1:c.13322C= XP_016867972.1:p.Thr4441=
XM_017012484.1:c.13292C= XP_016867973.1:p.Thr4431=
XM_017012485.1:c.13274C= XP_016867974.1:p.Thr4425=
XM_017012486.1:c.13250C= XP_016867975.1:p.Thr4417=
XM_017012487.1:c.13178C= XP_016867976.1:p.Thr4393=
XM_017012488.1:c.13142C= XP_016867977.1:p.Thr4381=
XM_017012489.1:c.9995C= XP_016867978.1:p.Thr3332=
XM_017012490.2:c.9599C= XP_016867979.1:p.Thr3200=
XM_024446852.1:c.13322C= XP_024302620.1:p.Thr4441=
XM_024446853.1:c.13250C= XP_024302621.1:p.Thr4417=
NM_170606.3:c.13109C= MANE Select NP_733751.2:p.Thr4370=