Canonical Allele Identifier: CA458884964

Gene: KMT2C

Linked Data

• MyVariant Identifiers: chr7:g.151845767T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.152148682T>A , CM000669.2:g.152148682T>A	GRCh38
NC_000007.13:g.151845767T>A , CM000669.1:g.151845767T>A	GRCh37
NC_000007.12:g.151476700T>A	NCBI36
NG_033948.1:g.292324A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000682040.1:c.1433A>T
ENST00000682116.1:n.2377A>T
ENST00000682283.1:c.13416A>T	ENSP00000507485.1:p.Gly4472=
ENST00000682629.1:n.2545A>T
ENST00000683120.1:n.8437A>T
ENST00000683178.1:c.3818A>T
ENST00000683200.1:c.10755A>T	ENSP00000508052.1:p.Gly3585=
ENST00000683337.1:n.4875A>T
ENST00000683502.1:c.3890A>T
ENST00000683621.1:n.2011A>T
ENST00000683640.1:n.1961A>T
ENST00000684069.1:c.1662A>T	ENSP00000507650.1:p.Gly554=
ENST00000684261.1:c.8142A>T	ENSP00000508097.1:p.Gly2714=
ENST00000684391.1:n.3A>T
ENST00000684649.1:c.3890A>T
ENST00000262189.11:c.13245A>T MANE Select	ENSP00000262189.6:p.Gly4415=
ENST00000360104.8:c.9032A>T
ENST00000418061.2:c.3887A>T
ENST00000424877.6:c.3821A>T
ENST00000679393.1:n.7956A>T
ENST00000679560.1:c.8145A>T	ENSP00000505094.1:p.Gly2715=
ENST00000679882.1:c.12810A>T	ENSP00000506154.1:p.Gly4270=
ENST00000680029.1:c.3822A>T
ENST00000680877.1:c.8145A>T	ENSP00000505724.1:p.Gly2715=
ENST00000681923.1:n.2260A>T
ENST00000262189.10:c.13245A>T	ENSP00000262189.6:p.Gly4415=
ENST00000355193.6:c.13245A>T	ENSP00000347325.3:p.Gly4415=
ENST00000360104.7:c.5926A>T
ENST00000424877.5:c.3096A>T	ENSP00000410411.1:p.Gly1032=
ENST00000473186.5:n.11127A>T
ENST00000558084.5:c.*10765A>T	ENSP00000453752.1:n.*10765A>T
NM_170606.2:c.13245A>T	NP_733751.2:p.Gly4415=
XM_005250025.3:c.13461A>T	XP_005250082.1:p.Gly4487=
XM_005250026.2:c.13458A>T	XP_005250083.1:p.Gly4486=
XM_005250027.3:c.13458A>T	XP_005250084.1:p.Gly4486=
XM_005250028.3:c.13461A>T	XP_005250085.1:p.Gly4487=
XM_005250031.3:c.13296A>T	XP_005250088.1:p.Gly4432=
XM_006716077.2:c.13458A>T	XP_006716140.1:p.Gly4486=
XM_006716078.2:c.13389A>T	XP_006716141.1:p.Gly4463=
XM_006716079.2:c.13293A>T	XP_006716142.1:p.Gly4431=
XM_011516450.1:c.13413A>T	XP_011514752.1:p.Gly4471=
XM_011516451.1:c.13341A>T	XP_011514753.1:p.Gly4447=
XM_011516452.1:c.13308A>T	XP_011514754.1:p.Gly4436=
XM_011516453.1:c.13224A>T	XP_011514755.1:p.Gly4408=
XM_011516454.1:c.12546A>T	XP_011514756.1:p.Gly4182=
XM_011516455.1:c.11007A>T	XP_011514757.1:p.Gly3669=
XM_011516456.1:c.13413A>T	XP_011514758.1:p.Gly4471=
XM_005250025.4:c.13461A>T	XP_005250082.1:p.Gly4487=
XM_005250026.3:c.13458A>T	XP_005250083.1:p.Gly4486=
XM_005250027.4:c.13458A>T	XP_005250084.1:p.Gly4486=
XM_005250028.4:c.13461A>T	XP_005250085.1:p.Gly4487=
XM_005250031.4:c.13296A>T	XP_005250088.1:p.Gly4432=
XM_006716077.3:c.13458A>T	XP_006716140.1:p.Gly4486=
XM_006716078.3:c.13389A>T	XP_006716141.1:p.Gly4463=
XM_006716079.3:c.13293A>T	XP_006716142.1:p.Gly4431=
XM_011516450.2:c.13413A>T	XP_011514752.1:p.Gly4471=
XM_011516451.2:c.13341A>T	XP_011514753.1:p.Gly4447=
XM_011516452.2:c.13308A>T	XP_011514754.1:p.Gly4436=
XM_011516453.2:c.13224A>T	XP_011514755.1:p.Gly4408=
XM_011516454.2:c.12546A>T	XP_011514756.1:p.Gly4182=
XM_011516456.2:c.13413A>T	XP_011514758.1:p.Gly4471=
XM_017012480.1:c.13461A>T	XP_016867969.1:p.Gly4487=
XM_017012481.1:c.13458A>T	XP_016867970.1:p.Gly4486=
XM_017012482.1:c.13458A>T	XP_016867971.1:p.Gly4486=
XM_017012483.1:c.13458A>T	XP_016867972.1:p.Gly4486=
XM_017012484.1:c.13428A>T	XP_016867973.1:p.Gly4476=
XM_017012485.1:c.13410A>T	XP_016867974.1:p.Gly4470=
XM_017012486.1:c.13386A>T	XP_016867975.1:p.Gly4462=
XM_017012487.1:c.13314A>T	XP_016867976.1:p.Gly4438=
XM_017012488.1:c.13278A>T	XP_016867977.1:p.Gly4426=
XM_017012489.1:c.10131A>T	XP_016867978.1:p.Gly3377=
XM_017012490.2:c.9735A>T	XP_016867979.1:p.Gly3245=
XM_024446852.1:c.13458A>T	XP_024302620.1:p.Gly4486=
XM_024446853.1:c.13386A>T	XP_024302621.1:p.Gly4462=
NM_170606.3:c.13245A>T MANE Select	NP_733751.2:p.Gly4415=