Canonical Allele Identifier: CA1752986356
Gene: KMT2C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152148798C= , CM000669.2:g.152148798C= GRCh38
NC_000007.13:g.151845883C= , CM000669.1:g.151845883C= GRCh37
NC_000007.12:g.151476816C= NCBI36
NG_033948.1:g.292208G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682040.1:c.1317G=
ENST00000682116.1:n.2261G=
ENST00000682283.1:c.13300G= ENSP00000507485.1:p.Asp4434=
ENST00000682629.1:n.2429G=
ENST00000683120.1:n.8321G=
ENST00000683178.1:c.3702G=
ENST00000683200.1:c.10639G= ENSP00000508052.1:p.Asp3547=
ENST00000683337.1:n.4759G=
ENST00000683502.1:c.3774G=
ENST00000683621.1:n.1895G=
ENST00000683640.1:n.1845G=
ENST00000684069.1:c.1546G= ENSP00000507650.1:p.Asp516=
ENST00000684261.1:c.8026G= ENSP00000508097.1:p.Asp2676=
ENST00000684649.1:c.3774G=
ENST00000262189.11:c.13129G= MANE Select ENSP00000262189.6:p.Asp4377=
ENST00000360104.8:c.8916G=
ENST00000418061.2:c.3771G=
ENST00000424877.6:c.3705G=
ENST00000679393.1:n.7840G=
ENST00000679560.1:c.8029G= ENSP00000505094.1:p.Asp2677=
ENST00000679882.1:c.12694G= ENSP00000506154.1:p.Asp4232=
ENST00000680029.1:c.3706G=
ENST00000680877.1:c.8029G= ENSP00000505724.1:p.Asp2677=
ENST00000681923.1:n.2144G=
ENST00000262189.10:c.13129G= ENSP00000262189.6:p.Asp4377=
ENST00000355193.6:c.13129G= ENSP00000347325.3:p.Asp4377=
ENST00000360104.7:c.5810G=
ENST00000424877.5:c.2980G= ENSP00000410411.1:p.Asp994=
ENST00000473186.5:n.11011G=
ENST00000558084.5:c.*10649G= ENSP00000453752.1:n.*10649G=
NM_170606.2:c.13129G= NP_733751.2:p.Asp4377=
XM_005250025.3:c.13345G= XP_005250082.1:p.Asp4449=
XM_005250026.2:c.13342G= XP_005250083.1:p.Asp4448=
XM_005250027.3:c.13342G= XP_005250084.1:p.Asp4448=
XM_005250028.3:c.13345G= XP_005250085.1:p.Asp4449=
XM_005250031.3:c.13180G= XP_005250088.1:p.Asp4394=
XM_006716077.2:c.13342G= XP_006716140.1:p.Asp4448=
XM_006716078.2:c.13273G= XP_006716141.1:p.Asp4425=
XM_006716079.2:c.13177G= XP_006716142.1:p.Asp4393=
XM_011516450.1:c.13297G= XP_011514752.1:p.Asp4433=
XM_011516451.1:c.13225G= XP_011514753.1:p.Asp4409=
XM_011516452.1:c.13192G= XP_011514754.1:p.Asp4398=
XM_011516453.1:c.13108G= XP_011514755.1:p.Asp4370=
XM_011516454.1:c.12430G= XP_011514756.1:p.Asp4144=
XM_011516455.1:c.10891G= XP_011514757.1:p.Asp3631=
XM_011516456.1:c.13297G= XP_011514758.1:p.Asp4433=
XM_005250025.4:c.13345G= XP_005250082.1:p.Asp4449=
XM_005250026.3:c.13342G= XP_005250083.1:p.Asp4448=
XM_005250027.4:c.13342G= XP_005250084.1:p.Asp4448=
XM_005250028.4:c.13345G= XP_005250085.1:p.Asp4449=
XM_005250031.4:c.13180G= XP_005250088.1:p.Asp4394=
XM_006716077.3:c.13342G= XP_006716140.1:p.Asp4448=
XM_006716078.3:c.13273G= XP_006716141.1:p.Asp4425=
XM_006716079.3:c.13177G= XP_006716142.1:p.Asp4393=
XM_011516450.2:c.13297G= XP_011514752.1:p.Asp4433=
XM_011516451.2:c.13225G= XP_011514753.1:p.Asp4409=
XM_011516452.2:c.13192G= XP_011514754.1:p.Asp4398=
XM_011516453.2:c.13108G= XP_011514755.1:p.Asp4370=
XM_011516454.2:c.12430G= XP_011514756.1:p.Asp4144=
XM_011516456.2:c.13297G= XP_011514758.1:p.Asp4433=
XM_017012480.1:c.13345G= XP_016867969.1:p.Asp4449=
XM_017012481.1:c.13342G= XP_016867970.1:p.Asp4448=
XM_017012482.1:c.13342G= XP_016867971.1:p.Asp4448=
XM_017012483.1:c.13342G= XP_016867972.1:p.Asp4448=
XM_017012484.1:c.13312G= XP_016867973.1:p.Asp4438=
XM_017012485.1:c.13294G= XP_016867974.1:p.Asp4432=
XM_017012486.1:c.13270G= XP_016867975.1:p.Asp4424=
XM_017012487.1:c.13198G= XP_016867976.1:p.Asp4400=
XM_017012488.1:c.13162G= XP_016867977.1:p.Asp4388=
XM_017012489.1:c.10015G= XP_016867978.1:p.Asp3339=
XM_017012490.2:c.9619G= XP_016867979.1:p.Asp3207=
XM_024446852.1:c.13342G= XP_024302620.1:p.Asp4448=
XM_024446853.1:c.13270G= XP_024302621.1:p.Asp4424=
NM_170606.3:c.13129G= MANE Select NP_733751.2:p.Asp4377=