Canonical Allele Identifier: CA1752986299
Gene: KMT2C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152148776T= , CM000669.2:g.152148776T= GRCh38
NC_000007.13:g.151845861T= , CM000669.1:g.151845861T= GRCh37
NC_000007.12:g.151476794T= NCBI36
NG_033948.1:g.292230A=

Transcript Alleles

HGVS Amino-acid change
ENST00000682040.1:c.1339A=
ENST00000682116.1:n.2283A=
ENST00000682283.1:c.13322A= ENSP00000507485.1:p.Lys4441=
ENST00000682629.1:n.2451A=
ENST00000683120.1:n.8343A=
ENST00000683178.1:c.3724A=
ENST00000683200.1:c.10661A= ENSP00000508052.1:p.Lys3554=
ENST00000683337.1:n.4781A=
ENST00000683502.1:c.3796A=
ENST00000683621.1:n.1917A=
ENST00000683640.1:n.1867A=
ENST00000684069.1:c.1568A= ENSP00000507650.1:p.Lys523=
ENST00000684261.1:c.8048A= ENSP00000508097.1:p.Lys2683=
ENST00000684649.1:c.3796A=
ENST00000262189.11:c.13151A= MANE Select ENSP00000262189.6:p.Lys4384=
ENST00000360104.8:c.8938A=
ENST00000418061.2:c.3793A=
ENST00000424877.6:c.3727A=
ENST00000679393.1:n.7862A=
ENST00000679560.1:c.8051A= ENSP00000505094.1:p.Lys2684=
ENST00000679882.1:c.12716A= ENSP00000506154.1:p.Lys4239=
ENST00000680029.1:c.3728A=
ENST00000680877.1:c.8051A= ENSP00000505724.1:p.Lys2684=
ENST00000681923.1:n.2166A=
ENST00000262189.10:c.13151A= ENSP00000262189.6:p.Lys4384=
ENST00000355193.6:c.13151A= ENSP00000347325.3:p.Lys4384=
ENST00000360104.7:c.5832A=
ENST00000424877.5:c.3002A= ENSP00000410411.1:p.Lys1001=
ENST00000473186.5:n.11033A=
ENST00000558084.5:c.*10671A= ENSP00000453752.1:n.*10671A=
NM_170606.2:c.13151A= NP_733751.2:p.Lys4384=
XM_005250025.3:c.13367A= XP_005250082.1:p.Lys4456=
XM_005250026.2:c.13364A= XP_005250083.1:p.Lys4455=
XM_005250027.3:c.13364A= XP_005250084.1:p.Lys4455=
XM_005250028.3:c.13367A= XP_005250085.1:p.Lys4456=
XM_005250031.3:c.13202A= XP_005250088.1:p.Lys4401=
XM_006716077.2:c.13364A= XP_006716140.1:p.Lys4455=
XM_006716078.2:c.13295A= XP_006716141.1:p.Lys4432=
XM_006716079.2:c.13199A= XP_006716142.1:p.Lys4400=
XM_011516450.1:c.13319A= XP_011514752.1:p.Lys4440=
XM_011516451.1:c.13247A= XP_011514753.1:p.Lys4416=
XM_011516452.1:c.13214A= XP_011514754.1:p.Lys4405=
XM_011516453.1:c.13130A= XP_011514755.1:p.Lys4377=
XM_011516454.1:c.12452A= XP_011514756.1:p.Lys4151=
XM_011516455.1:c.10913A= XP_011514757.1:p.Lys3638=
XM_011516456.1:c.13319A= XP_011514758.1:p.Lys4440=
XM_005250025.4:c.13367A= XP_005250082.1:p.Lys4456=
XM_005250026.3:c.13364A= XP_005250083.1:p.Lys4455=
XM_005250027.4:c.13364A= XP_005250084.1:p.Lys4455=
XM_005250028.4:c.13367A= XP_005250085.1:p.Lys4456=
XM_005250031.4:c.13202A= XP_005250088.1:p.Lys4401=
XM_006716077.3:c.13364A= XP_006716140.1:p.Lys4455=
XM_006716078.3:c.13295A= XP_006716141.1:p.Lys4432=
XM_006716079.3:c.13199A= XP_006716142.1:p.Lys4400=
XM_011516450.2:c.13319A= XP_011514752.1:p.Lys4440=
XM_011516451.2:c.13247A= XP_011514753.1:p.Lys4416=
XM_011516452.2:c.13214A= XP_011514754.1:p.Lys4405=
XM_011516453.2:c.13130A= XP_011514755.1:p.Lys4377=
XM_011516454.2:c.12452A= XP_011514756.1:p.Lys4151=
XM_011516456.2:c.13319A= XP_011514758.1:p.Lys4440=
XM_017012480.1:c.13367A= XP_016867969.1:p.Lys4456=
XM_017012481.1:c.13364A= XP_016867970.1:p.Lys4455=
XM_017012482.1:c.13364A= XP_016867971.1:p.Lys4455=
XM_017012483.1:c.13364A= XP_016867972.1:p.Lys4455=
XM_017012484.1:c.13334A= XP_016867973.1:p.Lys4445=
XM_017012485.1:c.13316A= XP_016867974.1:p.Lys4439=
XM_017012486.1:c.13292A= XP_016867975.1:p.Lys4431=
XM_017012487.1:c.13220A= XP_016867976.1:p.Lys4407=
XM_017012488.1:c.13184A= XP_016867977.1:p.Lys4395=
XM_017012489.1:c.10037A= XP_016867978.1:p.Lys3346=
XM_017012490.2:c.9641A= XP_016867979.1:p.Lys3214=
XM_024446852.1:c.13364A= XP_024302620.1:p.Lys4455=
XM_024446853.1:c.13292A= XP_024302621.1:p.Lys4431=
NM_170606.3:c.13151A= MANE Select NP_733751.2:p.Lys4384=