Canonical Allele Identifier: CA1752986463
Gene: KMT2C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152148866C= , CM000669.2:g.152148866C= GRCh38
NC_000007.13:g.151845951C= , CM000669.1:g.151845951C= GRCh37
NC_000007.12:g.151476884C= NCBI36
NG_033948.1:g.292140G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682040.1:c.1249G=
ENST00000682116.1:n.2193G=
ENST00000682283.1:c.13232G= ENSP00000507485.1:p.Gly4411=
ENST00000682629.1:n.2361G=
ENST00000683120.1:n.8253G=
ENST00000683178.1:c.3634G=
ENST00000683200.1:c.10571G= ENSP00000508052.1:p.Gly3524=
ENST00000683337.1:n.4691G=
ENST00000683502.1:c.3706G=
ENST00000683621.1:n.1827G=
ENST00000683640.1:n.1777G=
ENST00000684069.1:c.1478G= ENSP00000507650.1:p.Gly493=
ENST00000684261.1:c.7958G= ENSP00000508097.1:p.Gly2653=
ENST00000684649.1:c.3706G=
ENST00000262189.11:c.13061G= MANE Select ENSP00000262189.6:p.Gly4354=
ENST00000360104.8:c.8848G=
ENST00000418061.2:c.3703G=
ENST00000424877.6:c.3637G=
ENST00000679393.1:n.7772G=
ENST00000679560.1:c.7961G= ENSP00000505094.1:p.Gly2654=
ENST00000679882.1:c.12626G= ENSP00000506154.1:p.Gly4209=
ENST00000680029.1:c.3638G=
ENST00000680877.1:c.7961G= ENSP00000505724.1:p.Gly2654=
ENST00000681923.1:n.2076G=
ENST00000262189.10:c.13061G= ENSP00000262189.6:p.Gly4354=
ENST00000355193.6:c.13061G= ENSP00000347325.3:p.Gly4354=
ENST00000360104.7:c.5742G=
ENST00000424877.5:c.2912G= ENSP00000410411.1:p.Gly971=
ENST00000473186.5:n.10943G=
ENST00000558084.5:c.*10581G= ENSP00000453752.1:n.*10581G=
NM_170606.2:c.13061G= NP_733751.2:p.Gly4354=
XM_005250025.3:c.13277G= XP_005250082.1:p.Gly4426=
XM_005250026.2:c.13274G= XP_005250083.1:p.Gly4425=
XM_005250027.3:c.13274G= XP_005250084.1:p.Gly4425=
XM_005250028.3:c.13277G= XP_005250085.1:p.Gly4426=
XM_005250031.3:c.13112G= XP_005250088.1:p.Gly4371=
XM_006716077.2:c.13274G= XP_006716140.1:p.Gly4425=
XM_006716078.2:c.13205G= XP_006716141.1:p.Gly4402=
XM_006716079.2:c.13109G= XP_006716142.1:p.Gly4370=
XM_011516450.1:c.13229G= XP_011514752.1:p.Gly4410=
XM_011516451.1:c.13157G= XP_011514753.1:p.Gly4386=
XM_011516452.1:c.13124G= XP_011514754.1:p.Gly4375=
XM_011516453.1:c.13040G= XP_011514755.1:p.Gly4347=
XM_011516454.1:c.12362G= XP_011514756.1:p.Gly4121=
XM_011516455.1:c.10823G= XP_011514757.1:p.Gly3608=
XM_011516456.1:c.13229G= XP_011514758.1:p.Gly4410=
XM_005250025.4:c.13277G= XP_005250082.1:p.Gly4426=
XM_005250026.3:c.13274G= XP_005250083.1:p.Gly4425=
XM_005250027.4:c.13274G= XP_005250084.1:p.Gly4425=
XM_005250028.4:c.13277G= XP_005250085.1:p.Gly4426=
XM_005250031.4:c.13112G= XP_005250088.1:p.Gly4371=
XM_006716077.3:c.13274G= XP_006716140.1:p.Gly4425=
XM_006716078.3:c.13205G= XP_006716141.1:p.Gly4402=
XM_006716079.3:c.13109G= XP_006716142.1:p.Gly4370=
XM_011516450.2:c.13229G= XP_011514752.1:p.Gly4410=
XM_011516451.2:c.13157G= XP_011514753.1:p.Gly4386=
XM_011516452.2:c.13124G= XP_011514754.1:p.Gly4375=
XM_011516453.2:c.13040G= XP_011514755.1:p.Gly4347=
XM_011516454.2:c.12362G= XP_011514756.1:p.Gly4121=
XM_011516456.2:c.13229G= XP_011514758.1:p.Gly4410=
XM_017012480.1:c.13277G= XP_016867969.1:p.Gly4426=
XM_017012481.1:c.13274G= XP_016867970.1:p.Gly4425=
XM_017012482.1:c.13274G= XP_016867971.1:p.Gly4425=
XM_017012483.1:c.13274G= XP_016867972.1:p.Gly4425=
XM_017012484.1:c.13244G= XP_016867973.1:p.Gly4415=
XM_017012485.1:c.13226G= XP_016867974.1:p.Gly4409=
XM_017012486.1:c.13202G= XP_016867975.1:p.Gly4401=
XM_017012487.1:c.13130G= XP_016867976.1:p.Gly4377=
XM_017012488.1:c.13094G= XP_016867977.1:p.Gly4365=
XM_017012489.1:c.9947G= XP_016867978.1:p.Gly3316=
XM_017012490.2:c.9551G= XP_016867979.1:p.Gly3184=
XM_024446852.1:c.13274G= XP_024302620.1:p.Gly4425=
XM_024446853.1:c.13202G= XP_024302621.1:p.Gly4401=
NM_170606.3:c.13061G= MANE Select NP_733751.2:p.Gly4354=