Canonical Allele Identifier: CA458884742

Gene: KMT2C

Linked Data

• MyVariant Identifiers: chr7:g.151845887A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.152148802A>G , CM000669.2:g.152148802A>G	GRCh38
NC_000007.13:g.151845887A>G , CM000669.1:g.151845887A>G	GRCh37
NC_000007.12:g.151476820A>G	NCBI36
NG_033948.1:g.292204T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682040.1:c.1313T>C
ENST00000682116.1:n.2257T>C
ENST00000682283.1:c.13296T>C	ENSP00000507485.1:p.Cys4432=
ENST00000682629.1:n.2425T>C
ENST00000683120.1:n.8317T>C
ENST00000683178.1:c.3698T>C
ENST00000683200.1:c.10635T>C	ENSP00000508052.1:p.Cys3545=
ENST00000683337.1:n.4755T>C
ENST00000683502.1:c.3770T>C
ENST00000683621.1:n.1891T>C
ENST00000683640.1:n.1841T>C
ENST00000684069.1:c.1542T>C	ENSP00000507650.1:p.Cys514=
ENST00000684261.1:c.8022T>C	ENSP00000508097.1:p.Cys2674=
ENST00000684649.1:c.3770T>C
ENST00000262189.11:c.13125T>C MANE Select	ENSP00000262189.6:p.Cys4375=
ENST00000360104.8:c.8912T>C
ENST00000418061.2:c.3767T>C
ENST00000424877.6:c.3701T>C
ENST00000679393.1:n.7836T>C
ENST00000679560.1:c.8025T>C	ENSP00000505094.1:p.Cys2675=
ENST00000679882.1:c.12690T>C	ENSP00000506154.1:p.Cys4230=
ENST00000680029.1:c.3702T>C
ENST00000680877.1:c.8025T>C	ENSP00000505724.1:p.Cys2675=
ENST00000681923.1:n.2140T>C
ENST00000262189.10:c.13125T>C	ENSP00000262189.6:p.Cys4375=
ENST00000355193.6:c.13125T>C	ENSP00000347325.3:p.Cys4375=
ENST00000360104.7:c.5806T>C
ENST00000424877.5:c.2976T>C	ENSP00000410411.1:p.Cys992=
ENST00000473186.5:n.11007T>C
ENST00000558084.5:c.*10645T>C	ENSP00000453752.1:n.*10645T>C
NM_170606.2:c.13125T>C	NP_733751.2:p.Cys4375=
XM_005250025.3:c.13341T>C	XP_005250082.1:p.Cys4447=
XM_005250026.2:c.13338T>C	XP_005250083.1:p.Cys4446=
XM_005250027.3:c.13338T>C	XP_005250084.1:p.Cys4446=
XM_005250028.3:c.13341T>C	XP_005250085.1:p.Cys4447=
XM_005250031.3:c.13176T>C	XP_005250088.1:p.Cys4392=
XM_006716077.2:c.13338T>C	XP_006716140.1:p.Cys4446=
XM_006716078.2:c.13269T>C	XP_006716141.1:p.Cys4423=
XM_006716079.2:c.13173T>C	XP_006716142.1:p.Cys4391=
XM_011516450.1:c.13293T>C	XP_011514752.1:p.Cys4431=
XM_011516451.1:c.13221T>C	XP_011514753.1:p.Cys4407=
XM_011516452.1:c.13188T>C	XP_011514754.1:p.Cys4396=
XM_011516453.1:c.13104T>C	XP_011514755.1:p.Cys4368=
XM_011516454.1:c.12426T>C	XP_011514756.1:p.Cys4142=
XM_011516455.1:c.10887T>C	XP_011514757.1:p.Cys3629=
XM_011516456.1:c.13293T>C	XP_011514758.1:p.Cys4431=
XM_005250025.4:c.13341T>C	XP_005250082.1:p.Cys4447=
XM_005250026.3:c.13338T>C	XP_005250083.1:p.Cys4446=
XM_005250027.4:c.13338T>C	XP_005250084.1:p.Cys4446=
XM_005250028.4:c.13341T>C	XP_005250085.1:p.Cys4447=
XM_005250031.4:c.13176T>C	XP_005250088.1:p.Cys4392=
XM_006716077.3:c.13338T>C	XP_006716140.1:p.Cys4446=
XM_006716078.3:c.13269T>C	XP_006716141.1:p.Cys4423=
XM_006716079.3:c.13173T>C	XP_006716142.1:p.Cys4391=
XM_011516450.2:c.13293T>C	XP_011514752.1:p.Cys4431=
XM_011516451.2:c.13221T>C	XP_011514753.1:p.Cys4407=
XM_011516452.2:c.13188T>C	XP_011514754.1:p.Cys4396=
XM_011516453.2:c.13104T>C	XP_011514755.1:p.Cys4368=
XM_011516454.2:c.12426T>C	XP_011514756.1:p.Cys4142=
XM_011516456.2:c.13293T>C	XP_011514758.1:p.Cys4431=
XM_017012480.1:c.13341T>C	XP_016867969.1:p.Cys4447=
XM_017012481.1:c.13338T>C	XP_016867970.1:p.Cys4446=
XM_017012482.1:c.13338T>C	XP_016867971.1:p.Cys4446=
XM_017012483.1:c.13338T>C	XP_016867972.1:p.Cys4446=
XM_017012484.1:c.13308T>C	XP_016867973.1:p.Cys4436=
XM_017012485.1:c.13290T>C	XP_016867974.1:p.Cys4430=
XM_017012486.1:c.13266T>C	XP_016867975.1:p.Cys4422=
XM_017012487.1:c.13194T>C	XP_016867976.1:p.Cys4398=
XM_017012488.1:c.13158T>C	XP_016867977.1:p.Cys4386=
XM_017012489.1:c.10011T>C	XP_016867978.1:p.Cys3337=
XM_017012490.2:c.9615T>C	XP_016867979.1:p.Cys3205=
XM_024446852.1:c.13338T>C	XP_024302620.1:p.Cys4446=
XM_024446853.1:c.13266T>C	XP_024302621.1:p.Cys4422=
NM_170606.3:c.13125T>C MANE Select	NP_733751.2:p.Cys4375=