Canonical Allele Identifier: CA458884902
Gene: KMT2C HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.151845950T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152148865T>G , CM000669.2:g.152148865T>G GRCh38
NC_000007.13:g.151845950T>G , CM000669.1:g.151845950T>G GRCh37
NC_000007.12:g.151476883T>G NCBI36
NG_033948.1:g.292141A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000682040.1:c.1250A>C
ENST00000682116.1:n.2194A>C
ENST00000682283.1:c.13233A>C ENSP00000507485.1:p.Gly4411=
ENST00000682629.1:n.2362A>C
ENST00000683120.1:n.8254A>C
ENST00000683178.1:c.3635A>C
ENST00000683200.1:c.10572A>C ENSP00000508052.1:p.Gly3524=
ENST00000683337.1:n.4692A>C
ENST00000683502.1:c.3707A>C
ENST00000683621.1:n.1828A>C
ENST00000683640.1:n.1778A>C
ENST00000684069.1:c.1479A>C ENSP00000507650.1:p.Gly493=
ENST00000684261.1:c.7959A>C ENSP00000508097.1:p.Gly2653=
ENST00000684649.1:c.3707A>C
ENST00000262189.11:c.13062A>C MANE Select ENSP00000262189.6:p.Gly4354=
ENST00000360104.8:c.8849A>C
ENST00000418061.2:c.3704A>C
ENST00000424877.6:c.3638A>C
ENST00000679393.1:n.7773A>C
ENST00000679560.1:c.7962A>C ENSP00000505094.1:p.Gly2654=
ENST00000679882.1:c.12627A>C ENSP00000506154.1:p.Gly4209=
ENST00000680029.1:c.3639A>C
ENST00000680877.1:c.7962A>C ENSP00000505724.1:p.Gly2654=
ENST00000681923.1:n.2077A>C
ENST00000262189.10:c.13062A>C ENSP00000262189.6:p.Gly4354=
ENST00000355193.6:c.13062A>C ENSP00000347325.3:p.Gly4354=
ENST00000360104.7:c.5743A>C
ENST00000424877.5:c.2913A>C ENSP00000410411.1:p.Gly971=
ENST00000473186.5:n.10944A>C
ENST00000558084.5:c.*10582A>C ENSP00000453752.1:n.*10582A>C
NM_170606.2:c.13062A>C NP_733751.2:p.Gly4354=
XM_005250025.3:c.13278A>C XP_005250082.1:p.Gly4426=
XM_005250026.2:c.13275A>C XP_005250083.1:p.Gly4425=
XM_005250027.3:c.13275A>C XP_005250084.1:p.Gly4425=
XM_005250028.3:c.13278A>C XP_005250085.1:p.Gly4426=
XM_005250031.3:c.13113A>C XP_005250088.1:p.Gly4371=
XM_006716077.2:c.13275A>C XP_006716140.1:p.Gly4425=
XM_006716078.2:c.13206A>C XP_006716141.1:p.Gly4402=
XM_006716079.2:c.13110A>C XP_006716142.1:p.Gly4370=
XM_011516450.1:c.13230A>C XP_011514752.1:p.Gly4410=
XM_011516451.1:c.13158A>C XP_011514753.1:p.Gly4386=
XM_011516452.1:c.13125A>C XP_011514754.1:p.Gly4375=
XM_011516453.1:c.13041A>C XP_011514755.1:p.Gly4347=
XM_011516454.1:c.12363A>C XP_011514756.1:p.Gly4121=
XM_011516455.1:c.10824A>C XP_011514757.1:p.Gly3608=
XM_011516456.1:c.13230A>C XP_011514758.1:p.Gly4410=
XM_005250025.4:c.13278A>C XP_005250082.1:p.Gly4426=
XM_005250026.3:c.13275A>C XP_005250083.1:p.Gly4425=
XM_005250027.4:c.13275A>C XP_005250084.1:p.Gly4425=
XM_005250028.4:c.13278A>C XP_005250085.1:p.Gly4426=
XM_005250031.4:c.13113A>C XP_005250088.1:p.Gly4371=
XM_006716077.3:c.13275A>C XP_006716140.1:p.Gly4425=
XM_006716078.3:c.13206A>C XP_006716141.1:p.Gly4402=
XM_006716079.3:c.13110A>C XP_006716142.1:p.Gly4370=
XM_011516450.2:c.13230A>C XP_011514752.1:p.Gly4410=
XM_011516451.2:c.13158A>C XP_011514753.1:p.Gly4386=
XM_011516452.2:c.13125A>C XP_011514754.1:p.Gly4375=
XM_011516453.2:c.13041A>C XP_011514755.1:p.Gly4347=
XM_011516454.2:c.12363A>C XP_011514756.1:p.Gly4121=
XM_011516456.2:c.13230A>C XP_011514758.1:p.Gly4410=
XM_017012480.1:c.13278A>C XP_016867969.1:p.Gly4426=
XM_017012481.1:c.13275A>C XP_016867970.1:p.Gly4425=
XM_017012482.1:c.13275A>C XP_016867971.1:p.Gly4425=
XM_017012483.1:c.13275A>C XP_016867972.1:p.Gly4425=
XM_017012484.1:c.13245A>C XP_016867973.1:p.Gly4415=
XM_017012485.1:c.13227A>C XP_016867974.1:p.Gly4409=
XM_017012486.1:c.13203A>C XP_016867975.1:p.Gly4401=
XM_017012487.1:c.13131A>C XP_016867976.1:p.Gly4377=
XM_017012488.1:c.13095A>C XP_016867977.1:p.Gly4365=
XM_017012489.1:c.9948A>C XP_016867978.1:p.Gly3316=
XM_017012490.2:c.9552A>C XP_016867979.1:p.Gly3184=
XM_024446852.1:c.13275A>C XP_024302620.1:p.Gly4425=
XM_024446853.1:c.13203A>C XP_024302621.1:p.Gly4401=
NM_170606.3:c.13062A>C MANE Select NP_733751.2:p.Gly4354=