Canonical Allele Identifier: CA370091850

Gene: KMT2C

Linked Data

• MyVariant Identifiers: chr7:g.151845768C>G (hg19) ; chr7:g.152148683C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.152148683C>G , CM000669.2:g.152148683C>G	GRCh38
NC_000007.13:g.151845768C>G , CM000669.1:g.151845768C>G	GRCh37
NC_000007.12:g.151476701C>G	NCBI36
NG_033948.1:g.292323G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000682040.1:c.1432G>C
ENST00000682116.1:n.2376G>C
ENST00000682283.1:c.13415G>C	ENSP00000507485.1:p.Gly4472Ala
ENST00000682629.1:n.2544G>C
ENST00000683120.1:n.8436G>C
ENST00000683178.1:c.3817G>C
ENST00000683200.1:c.10754G>C	ENSP00000508052.1:p.Gly3585Ala
ENST00000683337.1:n.4874G>C
ENST00000683502.1:c.3889G>C
ENST00000683621.1:n.2010G>C
ENST00000683640.1:n.1960G>C
ENST00000684069.1:c.1661G>C	ENSP00000507650.1:p.Gly554Ala
ENST00000684261.1:c.8141G>C	ENSP00000508097.1:p.Gly2714Ala
ENST00000684391.1:n.2G>C
ENST00000684649.1:c.3889G>C
ENST00000262189.11:c.13244G>C MANE Select	ENSP00000262189.6:p.Gly4415Ala
ENST00000360104.8:c.9031G>C
ENST00000418061.2:c.3886G>C
ENST00000424877.6:c.3820G>C
ENST00000679393.1:n.7955G>C
ENST00000679560.1:c.8144G>C	ENSP00000505094.1:p.Gly2715Ala
ENST00000679882.1:c.12809G>C	ENSP00000506154.1:p.Gly4270Ala
ENST00000680029.1:c.3821G>C
ENST00000680877.1:c.8144G>C	ENSP00000505724.1:p.Gly2715Ala
ENST00000681923.1:n.2259G>C
ENST00000262189.10:c.13244G>C	ENSP00000262189.6:p.Gly4415Ala
ENST00000355193.6:c.13244G>C	ENSP00000347325.3:p.Gly4415Ala
ENST00000360104.7:c.5925G>C
ENST00000424877.5:c.3095G>C	ENSP00000410411.1:p.Gly1032Ala
ENST00000473186.5:n.11126G>C
ENST00000558084.5:c.*10764G>C	ENSP00000453752.1:n.*10764G>C
NM_170606.2:c.13244G>C	NP_733751.2:p.Gly4415Ala
XM_005250025.3:c.13460G>C	XP_005250082.1:p.Gly4487Ala
XM_005250026.2:c.13457G>C	XP_005250083.1:p.Gly4486Ala
XM_005250027.3:c.13457G>C	XP_005250084.1:p.Gly4486Ala
XM_005250028.3:c.13460G>C	XP_005250085.1:p.Gly4487Ala
XM_005250031.3:c.13295G>C	XP_005250088.1:p.Gly4432Ala
XM_006716077.2:c.13457G>C	XP_006716140.1:p.Gly4486Ala
XM_006716078.2:c.13388G>C	XP_006716141.1:p.Gly4463Ala
XM_006716079.2:c.13292G>C	XP_006716142.1:p.Gly4431Ala
XM_011516450.1:c.13412G>C	XP_011514752.1:p.Gly4471Ala
XM_011516451.1:c.13340G>C	XP_011514753.1:p.Gly4447Ala
XM_011516452.1:c.13307G>C	XP_011514754.1:p.Gly4436Ala
XM_011516453.1:c.13223G>C	XP_011514755.1:p.Gly4408Ala
XM_011516454.1:c.12545G>C	XP_011514756.1:p.Gly4182Ala
XM_011516455.1:c.11006G>C	XP_011514757.1:p.Gly3669Ala
XM_011516456.1:c.13412G>C	XP_011514758.1:p.Gly4471Ala
XM_005250025.4:c.13460G>C	XP_005250082.1:p.Gly4487Ala
XM_005250026.3:c.13457G>C	XP_005250083.1:p.Gly4486Ala
XM_005250027.4:c.13457G>C	XP_005250084.1:p.Gly4486Ala
XM_005250028.4:c.13460G>C	XP_005250085.1:p.Gly4487Ala
XM_005250031.4:c.13295G>C	XP_005250088.1:p.Gly4432Ala
XM_006716077.3:c.13457G>C	XP_006716140.1:p.Gly4486Ala
XM_006716078.3:c.13388G>C	XP_006716141.1:p.Gly4463Ala
XM_006716079.3:c.13292G>C	XP_006716142.1:p.Gly4431Ala
XM_011516450.2:c.13412G>C	XP_011514752.1:p.Gly4471Ala
XM_011516451.2:c.13340G>C	XP_011514753.1:p.Gly4447Ala
XM_011516452.2:c.13307G>C	XP_011514754.1:p.Gly4436Ala
XM_011516453.2:c.13223G>C	XP_011514755.1:p.Gly4408Ala
XM_011516454.2:c.12545G>C	XP_011514756.1:p.Gly4182Ala
XM_011516456.2:c.13412G>C	XP_011514758.1:p.Gly4471Ala
XM_017012480.1:c.13460G>C	XP_016867969.1:p.Gly4487Ala
XM_017012481.1:c.13457G>C	XP_016867970.1:p.Gly4486Ala
XM_017012482.1:c.13457G>C	XP_016867971.1:p.Gly4486Ala
XM_017012483.1:c.13457G>C	XP_016867972.1:p.Gly4486Ala
XM_017012484.1:c.13427G>C	XP_016867973.1:p.Gly4476Ala
XM_017012485.1:c.13409G>C	XP_016867974.1:p.Gly4470Ala
XM_017012486.1:c.13385G>C	XP_016867975.1:p.Gly4462Ala
XM_017012487.1:c.13313G>C	XP_016867976.1:p.Gly4438Ala
XM_017012488.1:c.13277G>C	XP_016867977.1:p.Gly4426Ala
XM_017012489.1:c.10130G>C	XP_016867978.1:p.Gly3377Ala
XM_017012490.2:c.9734G>C	XP_016867979.1:p.Gly3245Ala
XM_024446852.1:c.13457G>C	XP_024302620.1:p.Gly4486Ala
XM_024446853.1:c.13385G>C	XP_024302621.1:p.Gly4462Ala
NM_170606.3:c.13244G>C MANE Select	NP_733751.2:p.Gly4415Ala