Canonical Allele Identifier: CA370106907
Community Standard Title: NM_170606.3(KMT2C):c.9559A>T (p.Thr3187Ser)
Gene: KMT2C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152167337T>A , CM000669.2:g.152167337T>A GRCh38
NC_000007.13:g.151864422T>A , CM000669.1:g.151864422T>A GRCh37
NC_000007.12:g.151495355T>A NCBI36
NG_033948.1:g.273669A>T

Transcript Alleles

HGVS Amino-acid Change
NM_170606.3:c.9559A>T MANE Select NP_733751.2:p.Thr3187Ser
ENST00000262189.11:c.9559A>T MANE Select ENSP00000262189.6:p.Thr3187Ser
NM_170606.2:c.9559A>T NP_733751.2:p.Thr3187Ser
ENST00000262189.10:c.9559A>T ENSP00000262189.6:p.Thr3187Ser
ENST00000355193.6:c.9559A>T ENSP00000347325.3:p.Thr3187Ser
ENST00000360104.7:c.2075A>T
ENST00000360104.8:c.5181A>T
ENST00000418061.2:c.42A>T
ENST00000424877.6:c.42A>T
ENST00000473186.5:n.7270A>T
ENST00000558084.5:c.*7079A>T ENSP00000453752.1:n.*7079A>T
ENST00000679393.1:n.3050A>T
ENST00000679560.1:c.4294A>T ENSP00000505094.1:p.Thr1432Ser
ENST00000679882.1:c.9334A>T ENSP00000506154.1:p.Thr3112Ser
ENST00000680029.1:c.42A>T
ENST00000680877.1:c.4294A>T ENSP00000505724.1:p.Thr1432Ser
ENST00000680969.1:c.6955A>T ENSP00000505951.1:p.Thr2319Ser
ENST00000682283.1:c.9559A>T ENSP00000507485.1:p.Thr3187Ser
ENST00000683120.1:n.1545A>T
ENST00000683178.1:c.42A>T
ENST00000683200.1:c.6907A>T ENSP00000508052.1:p.Thr2303Ser
ENST00000683397.1:c.4317A>T ENSP00000507053.1:p.Arg1439Ser
ENST00000683502.1:c.42A>T
ENST00000683625.1:c.4294A>T ENSP00000507769.1:p.Thr1432Ser
ENST00000683670.1:c.4294A>T ENSP00000507634.1:p.Thr1432Ser
ENST00000684261.1:c.4294A>T ENSP00000508097.1:p.Thr1432Ser
ENST00000684307.1:c.4230A>T ENSP00000507202.1:p.Arg1410Ser
ENST00000684398.1:c.4294A>T ENSP00000507254.1:p.Thr1432Ser
ENST00000684649.1:c.42A>T
XM_005250025.3:c.9610A>T XP_005250082.1:p.Thr3204Ser
XM_005250025.4:c.9610A>T XP_005250082.1:p.Thr3204Ser
XM_005250026.2:c.9607A>T XP_005250083.1:p.Thr3203Ser
XM_005250026.3:c.9607A>T XP_005250083.1:p.Thr3203Ser
XM_005250027.3:c.9610A>T XP_005250084.1:p.Thr3204Ser
XM_005250027.4:c.9610A>T XP_005250084.1:p.Thr3204Ser
XM_005250028.3:c.9610A>T XP_005250085.1:p.Thr3204Ser
XM_005250028.4:c.9610A>T XP_005250085.1:p.Thr3204Ser
XM_005250031.3:c.9610A>T XP_005250088.1:p.Thr3204Ser
XM_005250031.4:c.9610A>T XP_005250088.1:p.Thr3204Ser
XM_006716077.2:c.9610A>T XP_006716140.1:p.Thr3204Ser
XM_006716077.3:c.9610A>T XP_006716140.1:p.Thr3204Ser
XM_006716078.2:c.9610A>T XP_006716141.1:p.Thr3204Ser
XM_006716078.3:c.9610A>T XP_006716141.1:p.Thr3204Ser
XM_006716079.2:c.9610A>T XP_006716142.1:p.Thr3204Ser
XM_006716079.3:c.9610A>T XP_006716142.1:p.Thr3204Ser
XM_011516450.1:c.9562A>T XP_011514752.1:p.Thr3188Ser
XM_011516450.2:c.9562A>T XP_011514752.1:p.Thr3188Ser
XM_011516451.1:c.9490A>T XP_011514753.1:p.Thr3164Ser
XM_011516451.2:c.9490A>T XP_011514753.1:p.Thr3164Ser
XM_011516452.1:c.9457A>T XP_011514754.1:p.Thr3153Ser
XM_011516452.2:c.9457A>T XP_011514754.1:p.Thr3153Ser
XM_011516453.1:c.9610A>T XP_011514755.1:p.Thr3204Ser
XM_011516453.2:c.9610A>T XP_011514755.1:p.Thr3204Ser
XM_011516454.1:c.8695A>T XP_011514756.1:p.Thr2899Ser
XM_011516454.2:c.8695A>T XP_011514756.1:p.Thr2899Ser
XM_011516455.1:c.7156A>T XP_011514757.1:p.Thr2386Ser
XM_011516456.1:c.9562A>T XP_011514758.1:p.Thr3188Ser
XM_011516456.2:c.9562A>T XP_011514758.1:p.Thr3188Ser
XM_017012480.1:c.9610A>T XP_016867969.1:p.Thr3204Ser
XM_017012481.1:c.9607A>T XP_016867970.1:p.Thr3203Ser
XM_017012482.1:c.9610A>T XP_016867971.1:p.Thr3204Ser
XM_017012483.1:c.9610A>T XP_016867972.1:p.Thr3204Ser
XM_017012484.1:c.9577A>T XP_016867973.1:p.Thr3193Ser
XM_017012485.1:c.9559A>T XP_016867974.1:p.Thr3187Ser
XM_017012486.1:c.9610A>T XP_016867975.1:p.Thr3204Ser
XM_017012487.1:c.9463A>T XP_016867976.1:p.Thr3155Ser
XM_017012488.1:c.9427A>T XP_016867977.1:p.Thr3143Ser
XM_017012489.1:c.6280A>T XP_016867978.1:p.Thr2094Ser
XM_017012490.2:c.5884A>T XP_016867979.1:p.Thr1962Ser
XM_024446852.1:c.9607A>T XP_024302620.1:p.Thr3203Ser
XM_024446853.1:c.9610A>T XP_024302621.1:p.Thr3204Ser
XR_428183.2:n.9818A>T
XR_428183.3:n.9842A>T