Canonical Allele Identifier: CA1752986435
Gene: KMT2C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152148834C= , CM000669.2:g.152148834C= GRCh38
NC_000007.13:g.151845919C= , CM000669.1:g.151845919C= GRCh37
NC_000007.12:g.151476852C= NCBI36
NG_033948.1:g.292172G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682040.1:c.1281G=
ENST00000682116.1:n.2225G=
ENST00000682283.1:c.13264G= ENSP00000507485.1:p.Val4422=
ENST00000682629.1:n.2393G=
ENST00000683120.1:n.8285G=
ENST00000683178.1:c.3666G=
ENST00000683200.1:c.10603G= ENSP00000508052.1:p.Val3535=
ENST00000683337.1:n.4723G=
ENST00000683502.1:c.3738G=
ENST00000683621.1:n.1859G=
ENST00000683640.1:n.1809G=
ENST00000684069.1:c.1510G= ENSP00000507650.1:p.Val504=
ENST00000684261.1:c.7990G= ENSP00000508097.1:p.Val2664=
ENST00000684649.1:c.3738G=
ENST00000262189.11:c.13093G= MANE Select ENSP00000262189.6:p.Val4365=
ENST00000360104.8:c.8880G=
ENST00000418061.2:c.3735G=
ENST00000424877.6:c.3669G=
ENST00000679393.1:n.7804G=
ENST00000679560.1:c.7993G= ENSP00000505094.1:p.Val2665=
ENST00000679882.1:c.12658G= ENSP00000506154.1:p.Val4220=
ENST00000680029.1:c.3670G=
ENST00000680877.1:c.7993G= ENSP00000505724.1:p.Val2665=
ENST00000681923.1:n.2108G=
ENST00000262189.10:c.13093G= ENSP00000262189.6:p.Val4365=
ENST00000355193.6:c.13093G= ENSP00000347325.3:p.Val4365=
ENST00000360104.7:c.5774G=
ENST00000424877.5:c.2944G= ENSP00000410411.1:p.Val982=
ENST00000473186.5:n.10975G=
ENST00000558084.5:c.*10613G= ENSP00000453752.1:n.*10613G=
NM_170606.2:c.13093G= NP_733751.2:p.Val4365=
XM_005250025.3:c.13309G= XP_005250082.1:p.Val4437=
XM_005250026.2:c.13306G= XP_005250083.1:p.Val4436=
XM_005250027.3:c.13306G= XP_005250084.1:p.Val4436=
XM_005250028.3:c.13309G= XP_005250085.1:p.Val4437=
XM_005250031.3:c.13144G= XP_005250088.1:p.Val4382=
XM_006716077.2:c.13306G= XP_006716140.1:p.Val4436=
XM_006716078.2:c.13237G= XP_006716141.1:p.Val4413=
XM_006716079.2:c.13141G= XP_006716142.1:p.Val4381=
XM_011516450.1:c.13261G= XP_011514752.1:p.Val4421=
XM_011516451.1:c.13189G= XP_011514753.1:p.Val4397=
XM_011516452.1:c.13156G= XP_011514754.1:p.Val4386=
XM_011516453.1:c.13072G= XP_011514755.1:p.Val4358=
XM_011516454.1:c.12394G= XP_011514756.1:p.Val4132=
XM_011516455.1:c.10855G= XP_011514757.1:p.Val3619=
XM_011516456.1:c.13261G= XP_011514758.1:p.Val4421=
XM_005250025.4:c.13309G= XP_005250082.1:p.Val4437=
XM_005250026.3:c.13306G= XP_005250083.1:p.Val4436=
XM_005250027.4:c.13306G= XP_005250084.1:p.Val4436=
XM_005250028.4:c.13309G= XP_005250085.1:p.Val4437=
XM_005250031.4:c.13144G= XP_005250088.1:p.Val4382=
XM_006716077.3:c.13306G= XP_006716140.1:p.Val4436=
XM_006716078.3:c.13237G= XP_006716141.1:p.Val4413=
XM_006716079.3:c.13141G= XP_006716142.1:p.Val4381=
XM_011516450.2:c.13261G= XP_011514752.1:p.Val4421=
XM_011516451.2:c.13189G= XP_011514753.1:p.Val4397=
XM_011516452.2:c.13156G= XP_011514754.1:p.Val4386=
XM_011516453.2:c.13072G= XP_011514755.1:p.Val4358=
XM_011516454.2:c.12394G= XP_011514756.1:p.Val4132=
XM_011516456.2:c.13261G= XP_011514758.1:p.Val4421=
XM_017012480.1:c.13309G= XP_016867969.1:p.Val4437=
XM_017012481.1:c.13306G= XP_016867970.1:p.Val4436=
XM_017012482.1:c.13306G= XP_016867971.1:p.Val4436=
XM_017012483.1:c.13306G= XP_016867972.1:p.Val4436=
XM_017012484.1:c.13276G= XP_016867973.1:p.Val4426=
XM_017012485.1:c.13258G= XP_016867974.1:p.Val4420=
XM_017012486.1:c.13234G= XP_016867975.1:p.Val4412=
XM_017012487.1:c.13162G= XP_016867976.1:p.Val4388=
XM_017012488.1:c.13126G= XP_016867977.1:p.Val4376=
XM_017012489.1:c.9979G= XP_016867978.1:p.Val3327=
XM_017012490.2:c.9583G= XP_016867979.1:p.Val3195=
XM_024446852.1:c.13306G= XP_024302620.1:p.Val4436=
XM_024446853.1:c.13234G= XP_024302621.1:p.Val4412=
NM_170606.3:c.13093G= MANE Select NP_733751.2:p.Val4365=