Canonical Allele Identifier: CA458884737

Gene: KMT2C

Linked Data

• MyVariant Identifiers: chr7:g.151845884C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.152148799C>T , CM000669.2:g.152148799C>T	GRCh38
NC_000007.13:g.151845884C>T , CM000669.1:g.151845884C>T	GRCh37
NC_000007.12:g.151476817C>T	NCBI36
NG_033948.1:g.292207G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682040.1:c.1316G>A
ENST00000682116.1:n.2260G>A
ENST00000682283.1:c.13299G>A	ENSP00000507485.1:p.Glu4433=
ENST00000682629.1:n.2428G>A
ENST00000683120.1:n.8320G>A
ENST00000683178.1:c.3701G>A
ENST00000683200.1:c.10638G>A	ENSP00000508052.1:p.Glu3546=
ENST00000683337.1:n.4758G>A
ENST00000683502.1:c.3773G>A
ENST00000683621.1:n.1894G>A
ENST00000683640.1:n.1844G>A
ENST00000684069.1:c.1545G>A	ENSP00000507650.1:p.Glu515=
ENST00000684261.1:c.8025G>A	ENSP00000508097.1:p.Glu2675=
ENST00000684649.1:c.3773G>A
ENST00000262189.11:c.13128G>A MANE Select	ENSP00000262189.6:p.Glu4376=
ENST00000360104.8:c.8915G>A
ENST00000418061.2:c.3770G>A
ENST00000424877.6:c.3704G>A
ENST00000679393.1:n.7839G>A
ENST00000679560.1:c.8028G>A	ENSP00000505094.1:p.Glu2676=
ENST00000679882.1:c.12693G>A	ENSP00000506154.1:p.Glu4231=
ENST00000680029.1:c.3705G>A
ENST00000680877.1:c.8028G>A	ENSP00000505724.1:p.Glu2676=
ENST00000681923.1:n.2143G>A
ENST00000262189.10:c.13128G>A	ENSP00000262189.6:p.Glu4376=
ENST00000355193.6:c.13128G>A	ENSP00000347325.3:p.Glu4376=
ENST00000360104.7:c.5809G>A
ENST00000424877.5:c.2979G>A	ENSP00000410411.1:p.Glu993=
ENST00000473186.5:n.11010G>A
ENST00000558084.5:c.*10648G>A	ENSP00000453752.1:n.*10648G>A
NM_170606.2:c.13128G>A	NP_733751.2:p.Glu4376=
XM_005250025.3:c.13344G>A	XP_005250082.1:p.Glu4448=
XM_005250026.2:c.13341G>A	XP_005250083.1:p.Glu4447=
XM_005250027.3:c.13341G>A	XP_005250084.1:p.Glu4447=
XM_005250028.3:c.13344G>A	XP_005250085.1:p.Glu4448=
XM_005250031.3:c.13179G>A	XP_005250088.1:p.Glu4393=
XM_006716077.2:c.13341G>A	XP_006716140.1:p.Glu4447=
XM_006716078.2:c.13272G>A	XP_006716141.1:p.Glu4424=
XM_006716079.2:c.13176G>A	XP_006716142.1:p.Glu4392=
XM_011516450.1:c.13296G>A	XP_011514752.1:p.Glu4432=
XM_011516451.1:c.13224G>A	XP_011514753.1:p.Glu4408=
XM_011516452.1:c.13191G>A	XP_011514754.1:p.Glu4397=
XM_011516453.1:c.13107G>A	XP_011514755.1:p.Glu4369=
XM_011516454.1:c.12429G>A	XP_011514756.1:p.Glu4143=
XM_011516455.1:c.10890G>A	XP_011514757.1:p.Glu3630=
XM_011516456.1:c.13296G>A	XP_011514758.1:p.Glu4432=
XM_005250025.4:c.13344G>A	XP_005250082.1:p.Glu4448=
XM_005250026.3:c.13341G>A	XP_005250083.1:p.Glu4447=
XM_005250027.4:c.13341G>A	XP_005250084.1:p.Glu4447=
XM_005250028.4:c.13344G>A	XP_005250085.1:p.Glu4448=
XM_005250031.4:c.13179G>A	XP_005250088.1:p.Glu4393=
XM_006716077.3:c.13341G>A	XP_006716140.1:p.Glu4447=
XM_006716078.3:c.13272G>A	XP_006716141.1:p.Glu4424=
XM_006716079.3:c.13176G>A	XP_006716142.1:p.Glu4392=
XM_011516450.2:c.13296G>A	XP_011514752.1:p.Glu4432=
XM_011516451.2:c.13224G>A	XP_011514753.1:p.Glu4408=
XM_011516452.2:c.13191G>A	XP_011514754.1:p.Glu4397=
XM_011516453.2:c.13107G>A	XP_011514755.1:p.Glu4369=
XM_011516454.2:c.12429G>A	XP_011514756.1:p.Glu4143=
XM_011516456.2:c.13296G>A	XP_011514758.1:p.Glu4432=
XM_017012480.1:c.13344G>A	XP_016867969.1:p.Glu4448=
XM_017012481.1:c.13341G>A	XP_016867970.1:p.Glu4447=
XM_017012482.1:c.13341G>A	XP_016867971.1:p.Glu4447=
XM_017012483.1:c.13341G>A	XP_016867972.1:p.Glu4447=
XM_017012484.1:c.13311G>A	XP_016867973.1:p.Glu4437=
XM_017012485.1:c.13293G>A	XP_016867974.1:p.Glu4431=
XM_017012486.1:c.13269G>A	XP_016867975.1:p.Glu4423=
XM_017012487.1:c.13197G>A	XP_016867976.1:p.Glu4399=
XM_017012488.1:c.13161G>A	XP_016867977.1:p.Glu4387=
XM_017012489.1:c.10014G>A	XP_016867978.1:p.Glu3338=
XM_017012490.2:c.9618G>A	XP_016867979.1:p.Glu3206=
XM_024446852.1:c.13341G>A	XP_024302620.1:p.Glu4447=
XM_024446853.1:c.13269G>A	XP_024302621.1:p.Glu4423=
NM_170606.3:c.13128G>A MANE Select	NP_733751.2:p.Glu4376=