Canonical Allele Identifier: CA4579918

Gene: KMT2C

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.152180069G>A , CM000669.2:g.152180069G>A	GRCh38
NC_000007.13:g.151877154G>A , CM000669.1:g.151877154G>A	GRCh37
NC_000007.12:g.151508087G>A	NCBI36
NG_033948.1:g.260937C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_170606.3:c.7207C>T MANE Select	NP_733751.2:p.Arg2403Ter
ENST00000262189.11:c.7207C>T MANE Select	ENSP00000262189.6:p.Arg2403Ter
NM_170606.2:c.7207C>T	NP_733751.2:p.Arg2403Ter
ENST00000262189.10:c.7207C>T	ENSP00000262189.6:p.Arg2403Ter
ENST00000355193.6:c.7207C>T	ENSP00000347325.3:p.Arg2403Ter
ENST00000360104.8:c.2829C>T
ENST00000473186.5:n.4918C>T
ENST00000558084.5:c.*4727C>T	ENSP00000453752.1:n.*4727C>T
ENST00000558665.1:c.121C>T	ENSP00000454058.1:p.Arg41Ter
ENST00000558665.2:c.496C>T	ENSP00000454058.2:p.Arg166Ter
ENST00000679393.1:n.698C>T
ENST00000679560.1:c.1942C>T	ENSP00000505094.1:p.Arg648Ter
ENST00000679645.1:c.*3300C>T	ENSP00000505745.1:n.*3300C>T
ENST00000679882.1:c.6982C>T	ENSP00000506154.1:p.Arg2328Ter
ENST00000680877.1:c.1942C>T	ENSP00000505724.1:p.Arg648Ter
ENST00000680969.1:c.4603C>T	ENSP00000505951.1:p.Arg1535Ter
ENST00000681033.1:c.5905C>T	ENSP00000505058.1:p.Arg1969Ter
ENST00000682176.1:c.3926C>T
ENST00000682283.1:c.7207C>T	ENSP00000507485.1:p.Arg2403Ter
ENST00000683159.1:c.2517C>T
ENST00000683200.1:c.4555C>T	ENSP00000508052.1:p.Arg1519Ter
ENST00000683397.1:c.1942C>T	ENSP00000507053.1:p.Arg648Ter
ENST00000683625.1:c.1942C>T	ENSP00000507769.1:p.Arg648Ter
ENST00000683670.1:c.1942C>T	ENSP00000507634.1:p.Arg648Ter
ENST00000684261.1:c.1942C>T	ENSP00000508097.1:p.Arg648Ter
ENST00000684307.1:c.1942C>T	ENSP00000507202.1:p.Arg648Ter
ENST00000684398.1:c.1942C>T	ENSP00000507254.1:p.Arg648Ter
XM_005250025.3:c.7258C>T	XP_005250082.1:p.Arg2420Ter
XM_005250025.4:c.7258C>T	XP_005250082.1:p.Arg2420Ter
XM_005250026.2:c.7255C>T	XP_005250083.1:p.Arg2419Ter
XM_005250026.3:c.7255C>T	XP_005250083.1:p.Arg2419Ter
XM_005250027.3:c.7258C>T	XP_005250084.1:p.Arg2420Ter
XM_005250027.4:c.7258C>T	XP_005250084.1:p.Arg2420Ter
XM_005250028.3:c.7258C>T	XP_005250085.1:p.Arg2420Ter
XM_005250028.4:c.7258C>T	XP_005250085.1:p.Arg2420Ter
XM_005250031.3:c.7258C>T	XP_005250088.1:p.Arg2420Ter
XM_005250031.4:c.7258C>T	XP_005250088.1:p.Arg2420Ter
XM_006716077.2:c.7258C>T	XP_006716140.1:p.Arg2420Ter
XM_006716077.3:c.7258C>T	XP_006716140.1:p.Arg2420Ter
XM_006716078.2:c.7258C>T	XP_006716141.1:p.Arg2420Ter
XM_006716078.3:c.7258C>T	XP_006716141.1:p.Arg2420Ter
XM_006716079.2:c.7258C>T	XP_006716142.1:p.Arg2420Ter
XM_006716079.3:c.7258C>T	XP_006716142.1:p.Arg2420Ter
XM_011516450.1:c.7210C>T	XP_011514752.1:p.Arg2404Ter
XM_011516450.2:c.7210C>T	XP_011514752.1:p.Arg2404Ter
XM_011516451.1:c.7138C>T	XP_011514753.1:p.Arg2380Ter
XM_011516451.2:c.7138C>T	XP_011514753.1:p.Arg2380Ter
XM_011516452.1:c.7105C>T	XP_011514754.1:p.Arg2369Ter
XM_011516452.2:c.7105C>T	XP_011514754.1:p.Arg2369Ter
XM_011516453.1:c.7258C>T	XP_011514755.1:p.Arg2420Ter
XM_011516453.2:c.7258C>T	XP_011514755.1:p.Arg2420Ter
XM_011516454.1:c.6343C>T	XP_011514756.1:p.Arg2115Ter
XM_011516454.2:c.6343C>T	XP_011514756.1:p.Arg2115Ter
XM_011516455.1:c.4804C>T	XP_011514757.1:p.Arg1602Ter
XM_011516456.1:c.7210C>T	XP_011514758.1:p.Arg2404Ter
XM_011516456.2:c.7210C>T	XP_011514758.1:p.Arg2404Ter
XM_017012480.1:c.7258C>T	XP_016867969.1:p.Arg2420Ter
XM_017012481.1:c.7255C>T	XP_016867970.1:p.Arg2419Ter
XM_017012482.1:c.7258C>T	XP_016867971.1:p.Arg2420Ter
XM_017012483.1:c.7258C>T	XP_016867972.1:p.Arg2420Ter
XM_017012484.1:c.7225C>T	XP_016867973.1:p.Arg2409Ter
XM_017012485.1:c.7207C>T	XP_016867974.1:p.Arg2403Ter
XM_017012486.1:c.7258C>T	XP_016867975.1:p.Arg2420Ter
XM_017012487.1:c.7111C>T	XP_016867976.1:p.Arg2371Ter
XM_017012488.1:c.7075C>T	XP_016867977.1:p.Arg2359Ter
XM_017012489.1:c.3928C>T	XP_016867978.1:p.Arg1310Ter
XM_017012490.2:c.3532C>T	XP_016867979.1:p.Arg1178Ter
XM_024446852.1:c.7255C>T	XP_024302620.1:p.Arg2419Ter
XM_024446853.1:c.7258C>T	XP_024302621.1:p.Arg2420Ter
XR_428183.2:n.7466C>T
XR_428183.3:n.7490C>T