Canonical Allele Identifier: CA4579670
Community Standard Title: NM_170606.3(KMT2C):c.8471C>T (p.Thr2824Met)
Gene: KMT2C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152176982G>A , CM000669.2:g.152176982G>A GRCh38
NC_000007.13:g.151874067G>A , CM000669.1:g.151874067G>A GRCh37
NC_000007.12:g.151505000G>A NCBI36
NG_033948.1:g.264024C>T

Transcript Alleles

HGVS Amino-acid Change
NM_170606.3:c.8471C>T MANE Select NP_733751.2:p.Thr2824Met
ENST00000262189.11:c.8471C>T MANE Select ENSP00000262189.6:p.Thr2824Met
NM_170606.2:c.8471C>T NP_733751.2:p.Thr2824Met
ENST00000262189.10:c.8471C>T ENSP00000262189.6:p.Thr2824Met
ENST00000355193.6:c.8471C>T ENSP00000347325.3:p.Thr2824Met
ENST00000360104.7:c.987C>T
ENST00000360104.8:c.4093C>T
ENST00000473186.5:n.6182C>T
ENST00000558084.5:c.*5991C>T ENSP00000453752.1:n.*5991C>T
ENST00000558665.2:c.1760C>T ENSP00000454058.2:p.Thr587Met
ENST00000679393.1:n.1962C>T
ENST00000679560.1:c.3206C>T ENSP00000505094.1:p.Thr1069Met
ENST00000679882.1:c.8246C>T ENSP00000506154.1:p.Thr2749Met
ENST00000680877.1:c.3206C>T ENSP00000505724.1:p.Thr1069Met
ENST00000680969.1:c.5867C>T ENSP00000505951.1:p.Thr1956Met
ENST00000681033.1:c.7169C>T ENSP00000505058.1:p.Thr2390Met
ENST00000682176.1:c.5190C>T
ENST00000682283.1:c.8471C>T ENSP00000507485.1:p.Thr2824Met
ENST00000683120.1:n.457C>T
ENST00000683159.1:c.3781C>T
ENST00000683200.1:c.5819C>T ENSP00000508052.1:p.Thr1940Met
ENST00000683397.1:c.3206C>T ENSP00000507053.1:p.Thr1069Met
ENST00000683625.1:c.3206C>T ENSP00000507769.1:p.Thr1069Met
ENST00000683670.1:c.3206C>T ENSP00000507634.1:p.Thr1069Met
ENST00000684261.1:c.3206C>T ENSP00000508097.1:p.Thr1069Met
ENST00000684307.1:c.3206C>T ENSP00000507202.1:p.Thr1069Met
ENST00000684398.1:c.3206C>T ENSP00000507254.1:p.Thr1069Met
XM_005250025.3:c.8522C>T XP_005250082.1:p.Thr2841Met
XM_005250025.4:c.8522C>T XP_005250082.1:p.Thr2841Met
XM_005250026.2:c.8519C>T XP_005250083.1:p.Thr2840Met
XM_005250026.3:c.8519C>T XP_005250083.1:p.Thr2840Met
XM_005250027.3:c.8522C>T XP_005250084.1:p.Thr2841Met
XM_005250027.4:c.8522C>T XP_005250084.1:p.Thr2841Met
XM_005250028.3:c.8522C>T XP_005250085.1:p.Thr2841Met
XM_005250028.4:c.8522C>T XP_005250085.1:p.Thr2841Met
XM_005250031.3:c.8522C>T XP_005250088.1:p.Thr2841Met
XM_005250031.4:c.8522C>T XP_005250088.1:p.Thr2841Met
XM_006716077.2:c.8522C>T XP_006716140.1:p.Thr2841Met
XM_006716077.3:c.8522C>T XP_006716140.1:p.Thr2841Met
XM_006716078.2:c.8522C>T XP_006716141.1:p.Thr2841Met
XM_006716078.3:c.8522C>T XP_006716141.1:p.Thr2841Met
XM_006716079.2:c.8522C>T XP_006716142.1:p.Thr2841Met
XM_006716079.3:c.8522C>T XP_006716142.1:p.Thr2841Met
XM_011516450.1:c.8474C>T XP_011514752.1:p.Thr2825Met
XM_011516450.2:c.8474C>T XP_011514752.1:p.Thr2825Met
XM_011516451.1:c.8402C>T XP_011514753.1:p.Thr2801Met
XM_011516451.2:c.8402C>T XP_011514753.1:p.Thr2801Met
XM_011516452.1:c.8369C>T XP_011514754.1:p.Thr2790Met
XM_011516452.2:c.8369C>T XP_011514754.1:p.Thr2790Met
XM_011516453.1:c.8522C>T XP_011514755.1:p.Thr2841Met
XM_011516453.2:c.8522C>T XP_011514755.1:p.Thr2841Met
XM_011516454.1:c.7607C>T XP_011514756.1:p.Thr2536Met
XM_011516454.2:c.7607C>T XP_011514756.1:p.Thr2536Met
XM_011516455.1:c.6068C>T XP_011514757.1:p.Thr2023Met
XM_011516456.1:c.8474C>T XP_011514758.1:p.Thr2825Met
XM_011516456.2:c.8474C>T XP_011514758.1:p.Thr2825Met
XM_017012480.1:c.8522C>T XP_016867969.1:p.Thr2841Met
XM_017012481.1:c.8519C>T XP_016867970.1:p.Thr2840Met
XM_017012482.1:c.8522C>T XP_016867971.1:p.Thr2841Met
XM_017012483.1:c.8522C>T XP_016867972.1:p.Thr2841Met
XM_017012484.1:c.8489C>T XP_016867973.1:p.Thr2830Met
XM_017012485.1:c.8471C>T XP_016867974.1:p.Thr2824Met
XM_017012486.1:c.8522C>T XP_016867975.1:p.Thr2841Met
XM_017012487.1:c.8375C>T XP_016867976.1:p.Thr2792Met
XM_017012488.1:c.8339C>T XP_016867977.1:p.Thr2780Met
XM_017012489.1:c.5192C>T XP_016867978.1:p.Thr1731Met
XM_017012490.2:c.4796C>T XP_016867979.1:p.Thr1599Met
XM_024446852.1:c.8519C>T XP_024302620.1:p.Thr2840Met
XM_024446853.1:c.8522C>T XP_024302621.1:p.Thr2841Met
XR_428183.2:n.8730C>T
XR_428183.3:n.8754C>T