Canonical Allele Identifier: CA370093167

Gene: KMT2C

Linked Data

• MyVariant Identifiers: chr7:g.151845907C>G (hg19) ; chr7:g.152148822C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.152148822C>G , CM000669.2:g.152148822C>G	GRCh38
NC_000007.13:g.151845907C>G , CM000669.1:g.151845907C>G	GRCh37
NC_000007.12:g.151476840C>G	NCBI36
NG_033948.1:g.292184G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682040.1:c.1293G>C
ENST00000682116.1:n.2237G>C
ENST00000682283.1:c.13276G>C	ENSP00000507485.1:p.Gly4426Arg
ENST00000682629.1:n.2405G>C
ENST00000683120.1:n.8297G>C
ENST00000683178.1:c.3678G>C
ENST00000683200.1:c.10615G>C	ENSP00000508052.1:p.Gly3539Arg
ENST00000683337.1:n.4735G>C
ENST00000683502.1:c.3750G>C
ENST00000683621.1:n.1871G>C
ENST00000683640.1:n.1821G>C
ENST00000684069.1:c.1522G>C	ENSP00000507650.1:p.Gly508Arg
ENST00000684261.1:c.8002G>C	ENSP00000508097.1:p.Gly2668Arg
ENST00000684649.1:c.3750G>C
ENST00000262189.11:c.13105G>C MANE Select	ENSP00000262189.6:p.Gly4369Arg
ENST00000360104.8:c.8892G>C
ENST00000418061.2:c.3747G>C
ENST00000424877.6:c.3681G>C
ENST00000679393.1:n.7816G>C
ENST00000679560.1:c.8005G>C	ENSP00000505094.1:p.Gly2669Arg
ENST00000679882.1:c.12670G>C	ENSP00000506154.1:p.Gly4224Arg
ENST00000680029.1:c.3682G>C
ENST00000680877.1:c.8005G>C	ENSP00000505724.1:p.Gly2669Arg
ENST00000681923.1:n.2120G>C
ENST00000262189.10:c.13105G>C	ENSP00000262189.6:p.Gly4369Arg
ENST00000355193.6:c.13105G>C	ENSP00000347325.3:p.Gly4369Arg
ENST00000360104.7:c.5786G>C
ENST00000424877.5:c.2956G>C	ENSP00000410411.1:p.Gly986Arg
ENST00000473186.5:n.10987G>C
ENST00000558084.5:c.*10625G>C	ENSP00000453752.1:n.*10625G>C
NM_170606.2:c.13105G>C	NP_733751.2:p.Gly4369Arg
XM_005250025.3:c.13321G>C	XP_005250082.1:p.Gly4441Arg
XM_005250026.2:c.13318G>C	XP_005250083.1:p.Gly4440Arg
XM_005250027.3:c.13318G>C	XP_005250084.1:p.Gly4440Arg
XM_005250028.3:c.13321G>C	XP_005250085.1:p.Gly4441Arg
XM_005250031.3:c.13156G>C	XP_005250088.1:p.Gly4386Arg
XM_006716077.2:c.13318G>C	XP_006716140.1:p.Gly4440Arg
XM_006716078.2:c.13249G>C	XP_006716141.1:p.Gly4417Arg
XM_006716079.2:c.13153G>C	XP_006716142.1:p.Gly4385Arg
XM_011516450.1:c.13273G>C	XP_011514752.1:p.Gly4425Arg
XM_011516451.1:c.13201G>C	XP_011514753.1:p.Gly4401Arg
XM_011516452.1:c.13168G>C	XP_011514754.1:p.Gly4390Arg
XM_011516453.1:c.13084G>C	XP_011514755.1:p.Gly4362Arg
XM_011516454.1:c.12406G>C	XP_011514756.1:p.Gly4136Arg
XM_011516455.1:c.10867G>C	XP_011514757.1:p.Gly3623Arg
XM_011516456.1:c.13273G>C	XP_011514758.1:p.Gly4425Arg
XM_005250025.4:c.13321G>C	XP_005250082.1:p.Gly4441Arg
XM_005250026.3:c.13318G>C	XP_005250083.1:p.Gly4440Arg
XM_005250027.4:c.13318G>C	XP_005250084.1:p.Gly4440Arg
XM_005250028.4:c.13321G>C	XP_005250085.1:p.Gly4441Arg
XM_005250031.4:c.13156G>C	XP_005250088.1:p.Gly4386Arg
XM_006716077.3:c.13318G>C	XP_006716140.1:p.Gly4440Arg
XM_006716078.3:c.13249G>C	XP_006716141.1:p.Gly4417Arg
XM_006716079.3:c.13153G>C	XP_006716142.1:p.Gly4385Arg
XM_011516450.2:c.13273G>C	XP_011514752.1:p.Gly4425Arg
XM_011516451.2:c.13201G>C	XP_011514753.1:p.Gly4401Arg
XM_011516452.2:c.13168G>C	XP_011514754.1:p.Gly4390Arg
XM_011516453.2:c.13084G>C	XP_011514755.1:p.Gly4362Arg
XM_011516454.2:c.12406G>C	XP_011514756.1:p.Gly4136Arg
XM_011516456.2:c.13273G>C	XP_011514758.1:p.Gly4425Arg
XM_017012480.1:c.13321G>C	XP_016867969.1:p.Gly4441Arg
XM_017012481.1:c.13318G>C	XP_016867970.1:p.Gly4440Arg
XM_017012482.1:c.13318G>C	XP_016867971.1:p.Gly4440Arg
XM_017012483.1:c.13318G>C	XP_016867972.1:p.Gly4440Arg
XM_017012484.1:c.13288G>C	XP_016867973.1:p.Gly4430Arg
XM_017012485.1:c.13270G>C	XP_016867974.1:p.Gly4424Arg
XM_017012486.1:c.13246G>C	XP_016867975.1:p.Gly4416Arg
XM_017012487.1:c.13174G>C	XP_016867976.1:p.Gly4392Arg
XM_017012488.1:c.13138G>C	XP_016867977.1:p.Gly4380Arg
XM_017012489.1:c.9991G>C	XP_016867978.1:p.Gly3331Arg
XM_017012490.2:c.9595G>C	XP_016867979.1:p.Gly3199Arg
XM_024446852.1:c.13318G>C	XP_024302620.1:p.Gly4440Arg
XM_024446853.1:c.13246G>C	XP_024302621.1:p.Gly4416Arg
NM_170606.3:c.13105G>C MANE Select	NP_733751.2:p.Gly4369Arg