Canonical Allele Identifier: CA370091829

Gene: KMT2C

Linked Data

• MyVariant Identifiers: chr7:g.151845762G>A (hg19) ; chr7:g.152148677G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.152148677G>A , CM000669.2:g.152148677G>A	GRCh38
NC_000007.13:g.151845762G>A , CM000669.1:g.151845762G>A	GRCh37
NC_000007.12:g.151476695G>A	NCBI36
NG_033948.1:g.292329C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000682040.1:c.1438C>T
ENST00000682116.1:n.2382C>T
ENST00000682283.1:c.13421C>T	ENSP00000507485.1:p.Ala4474Val
ENST00000682629.1:n.2550C>T
ENST00000683120.1:n.8442C>T
ENST00000683178.1:c.3823C>T
ENST00000683200.1:c.10760C>T	ENSP00000508052.1:p.Ala3587Val
ENST00000683337.1:n.4880C>T
ENST00000683502.1:c.3895C>T
ENST00000683621.1:n.2016C>T
ENST00000683640.1:n.1966C>T
ENST00000684069.1:c.1667C>T	ENSP00000507650.1:p.Ala556Val
ENST00000684261.1:c.8147C>T	ENSP00000508097.1:p.Ala2716Val
ENST00000684391.1:n.8C>T
ENST00000684649.1:c.3895C>T
ENST00000262189.11:c.13250C>T MANE Select	ENSP00000262189.6:p.Ala4417Val
ENST00000360104.8:c.9037C>T
ENST00000418061.2:c.3892C>T
ENST00000424877.6:c.3826C>T
ENST00000679393.1:n.7961C>T
ENST00000679560.1:c.8150C>T	ENSP00000505094.1:p.Ala2717Val
ENST00000679882.1:c.12815C>T	ENSP00000506154.1:p.Ala4272Val
ENST00000680029.1:c.3827C>T
ENST00000680877.1:c.8150C>T	ENSP00000505724.1:p.Ala2717Val
ENST00000681923.1:n.2265C>T
ENST00000262189.10:c.13250C>T	ENSP00000262189.6:p.Ala4417Val
ENST00000355193.6:c.13250C>T	ENSP00000347325.3:p.Ala4417Val
ENST00000360104.7:c.5931C>T
ENST00000424877.5:c.3101C>T	ENSP00000410411.1:p.Ala1034Val
ENST00000473186.5:n.11132C>T
ENST00000558084.5:c.*10770C>T	ENSP00000453752.1:n.*10770C>T
NM_170606.2:c.13250C>T	NP_733751.2:p.Ala4417Val
XM_005250025.3:c.13466C>T	XP_005250082.1:p.Ala4489Val
XM_005250026.2:c.13463C>T	XP_005250083.1:p.Ala4488Val
XM_005250027.3:c.13463C>T	XP_005250084.1:p.Ala4488Val
XM_005250028.3:c.13466C>T	XP_005250085.1:p.Ala4489Val
XM_005250031.3:c.13301C>T	XP_005250088.1:p.Ala4434Val
XM_006716077.2:c.13463C>T	XP_006716140.1:p.Ala4488Val
XM_006716078.2:c.13394C>T	XP_006716141.1:p.Ala4465Val
XM_006716079.2:c.13298C>T	XP_006716142.1:p.Ala4433Val
XM_011516450.1:c.13418C>T	XP_011514752.1:p.Ala4473Val
XM_011516451.1:c.13346C>T	XP_011514753.1:p.Ala4449Val
XM_011516452.1:c.13313C>T	XP_011514754.1:p.Ala4438Val
XM_011516453.1:c.13229C>T	XP_011514755.1:p.Ala4410Val
XM_011516454.1:c.12551C>T	XP_011514756.1:p.Ala4184Val
XM_011516455.1:c.11012C>T	XP_011514757.1:p.Ala3671Val
XM_011516456.1:c.13418C>T	XP_011514758.1:p.Ala4473Val
XM_005250025.4:c.13466C>T	XP_005250082.1:p.Ala4489Val
XM_005250026.3:c.13463C>T	XP_005250083.1:p.Ala4488Val
XM_005250027.4:c.13463C>T	XP_005250084.1:p.Ala4488Val
XM_005250028.4:c.13466C>T	XP_005250085.1:p.Ala4489Val
XM_005250031.4:c.13301C>T	XP_005250088.1:p.Ala4434Val
XM_006716077.3:c.13463C>T	XP_006716140.1:p.Ala4488Val
XM_006716078.3:c.13394C>T	XP_006716141.1:p.Ala4465Val
XM_006716079.3:c.13298C>T	XP_006716142.1:p.Ala4433Val
XM_011516450.2:c.13418C>T	XP_011514752.1:p.Ala4473Val
XM_011516451.2:c.13346C>T	XP_011514753.1:p.Ala4449Val
XM_011516452.2:c.13313C>T	XP_011514754.1:p.Ala4438Val
XM_011516453.2:c.13229C>T	XP_011514755.1:p.Ala4410Val
XM_011516454.2:c.12551C>T	XP_011514756.1:p.Ala4184Val
XM_011516456.2:c.13418C>T	XP_011514758.1:p.Ala4473Val
XM_017012480.1:c.13466C>T	XP_016867969.1:p.Ala4489Val
XM_017012481.1:c.13463C>T	XP_016867970.1:p.Ala4488Val
XM_017012482.1:c.13463C>T	XP_016867971.1:p.Ala4488Val
XM_017012483.1:c.13463C>T	XP_016867972.1:p.Ala4488Val
XM_017012484.1:c.13433C>T	XP_016867973.1:p.Ala4478Val
XM_017012485.1:c.13415C>T	XP_016867974.1:p.Ala4472Val
XM_017012486.1:c.13391C>T	XP_016867975.1:p.Ala4464Val
XM_017012487.1:c.13319C>T	XP_016867976.1:p.Ala4440Val
XM_017012488.1:c.13283C>T	XP_016867977.1:p.Ala4428Val
XM_017012489.1:c.10136C>T	XP_016867978.1:p.Ala3379Val
XM_017012490.2:c.9740C>T	XP_016867979.1:p.Ala3247Val
XM_024446852.1:c.13463C>T	XP_024302620.1:p.Ala4488Val
XM_024446853.1:c.13391C>T	XP_024302621.1:p.Ala4464Val
NM_170606.3:c.13250C>T MANE Select	NP_733751.2:p.Ala4417Val