Canonical Allele Identifier: CA458884974

Gene: KMT2C

Linked Data

• MyVariant Identifiers: chr7:g.151845770A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.152148685A>G , CM000669.2:g.152148685A>G	GRCh38
NC_000007.13:g.151845770A>G , CM000669.1:g.151845770A>G	GRCh37
NC_000007.12:g.151476703A>G	NCBI36
NG_033948.1:g.292321T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000682040.1:c.1430T>C
ENST00000682116.1:n.2374T>C
ENST00000682283.1:c.13413T>C	ENSP00000507485.1:p.Asp4471=
ENST00000682629.1:n.2542T>C
ENST00000683120.1:n.8434T>C
ENST00000683178.1:c.3815T>C
ENST00000683200.1:c.10752T>C	ENSP00000508052.1:p.Asp3584=
ENST00000683337.1:n.4872T>C
ENST00000683502.1:c.3887T>C
ENST00000683621.1:n.2008T>C
ENST00000683640.1:n.1958T>C
ENST00000684069.1:c.1659T>C	ENSP00000507650.1:p.Asp553=
ENST00000684261.1:c.8139T>C	ENSP00000508097.1:p.Asp2713=
ENST00000684649.1:c.3887T>C
ENST00000262189.11:c.13242T>C MANE Select	ENSP00000262189.6:p.Asp4414=
ENST00000360104.8:c.9029T>C
ENST00000418061.2:c.3884T>C
ENST00000424877.6:c.3818T>C
ENST00000679393.1:n.7953T>C
ENST00000679560.1:c.8142T>C	ENSP00000505094.1:p.Asp2714=
ENST00000679882.1:c.12807T>C	ENSP00000506154.1:p.Asp4269=
ENST00000680029.1:c.3819T>C
ENST00000680877.1:c.8142T>C	ENSP00000505724.1:p.Asp2714=
ENST00000681923.1:n.2257T>C
ENST00000262189.10:c.13242T>C	ENSP00000262189.6:p.Asp4414=
ENST00000355193.6:c.13242T>C	ENSP00000347325.3:p.Asp4414=
ENST00000360104.7:c.5923T>C
ENST00000424877.5:c.3093T>C	ENSP00000410411.1:p.Asp1031=
ENST00000473186.5:n.11124T>C
ENST00000558084.5:c.*10762T>C	ENSP00000453752.1:n.*10762T>C
NM_170606.2:c.13242T>C	NP_733751.2:p.Asp4414=
XM_005250025.3:c.13458T>C	XP_005250082.1:p.Asp4486=
XM_005250026.2:c.13455T>C	XP_005250083.1:p.Asp4485=
XM_005250027.3:c.13455T>C	XP_005250084.1:p.Asp4485=
XM_005250028.3:c.13458T>C	XP_005250085.1:p.Asp4486=
XM_005250031.3:c.13293T>C	XP_005250088.1:p.Asp4431=
XM_006716077.2:c.13455T>C	XP_006716140.1:p.Asp4485=
XM_006716078.2:c.13386T>C	XP_006716141.1:p.Asp4462=
XM_006716079.2:c.13290T>C	XP_006716142.1:p.Asp4430=
XM_011516450.1:c.13410T>C	XP_011514752.1:p.Asp4470=
XM_011516451.1:c.13338T>C	XP_011514753.1:p.Asp4446=
XM_011516452.1:c.13305T>C	XP_011514754.1:p.Asp4435=
XM_011516453.1:c.13221T>C	XP_011514755.1:p.Asp4407=
XM_011516454.1:c.12543T>C	XP_011514756.1:p.Asp4181=
XM_011516455.1:c.11004T>C	XP_011514757.1:p.Asp3668=
XM_011516456.1:c.13410T>C	XP_011514758.1:p.Asp4470=
XM_005250025.4:c.13458T>C	XP_005250082.1:p.Asp4486=
XM_005250026.3:c.13455T>C	XP_005250083.1:p.Asp4485=
XM_005250027.4:c.13455T>C	XP_005250084.1:p.Asp4485=
XM_005250028.4:c.13458T>C	XP_005250085.1:p.Asp4486=
XM_005250031.4:c.13293T>C	XP_005250088.1:p.Asp4431=
XM_006716077.3:c.13455T>C	XP_006716140.1:p.Asp4485=
XM_006716078.3:c.13386T>C	XP_006716141.1:p.Asp4462=
XM_006716079.3:c.13290T>C	XP_006716142.1:p.Asp4430=
XM_011516450.2:c.13410T>C	XP_011514752.1:p.Asp4470=
XM_011516451.2:c.13338T>C	XP_011514753.1:p.Asp4446=
XM_011516452.2:c.13305T>C	XP_011514754.1:p.Asp4435=
XM_011516453.2:c.13221T>C	XP_011514755.1:p.Asp4407=
XM_011516454.2:c.12543T>C	XP_011514756.1:p.Asp4181=
XM_011516456.2:c.13410T>C	XP_011514758.1:p.Asp4470=
XM_017012480.1:c.13458T>C	XP_016867969.1:p.Asp4486=
XM_017012481.1:c.13455T>C	XP_016867970.1:p.Asp4485=
XM_017012482.1:c.13455T>C	XP_016867971.1:p.Asp4485=
XM_017012483.1:c.13455T>C	XP_016867972.1:p.Asp4485=
XM_017012484.1:c.13425T>C	XP_016867973.1:p.Asp4475=
XM_017012485.1:c.13407T>C	XP_016867974.1:p.Asp4469=
XM_017012486.1:c.13383T>C	XP_016867975.1:p.Asp4461=
XM_017012487.1:c.13311T>C	XP_016867976.1:p.Asp4437=
XM_017012488.1:c.13275T>C	XP_016867977.1:p.Asp4425=
XM_017012489.1:c.10128T>C	XP_016867978.1:p.Asp3376=
XM_017012490.2:c.9732T>C	XP_016867979.1:p.Asp3244=
XM_024446852.1:c.13455T>C	XP_024302620.1:p.Asp4485=
XM_024446853.1:c.13383T>C	XP_024302621.1:p.Asp4461=
NM_170606.3:c.13242T>C MANE Select	NP_733751.2:p.Asp4414=