Canonical Allele Identifier: CA370100544

Gene: KMT2C

Linked Data

• dbSNP Id: rs2129121627
• MyVariant Identifiers: chr7:g.151880231C>G (hg19) ; chr7:g.152183146C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.152183146C>G , CM000669.2:g.152183146C>G	GRCh38
NC_000007.13:g.151880231C>G , CM000669.1:g.151880231C>G	GRCh37
NC_000007.12:g.151511164C>G	NCBI36
NG_033948.1:g.257860G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000682176.1:c.1812G>C
ENST00000682283.1:c.5093G>C	ENSP00000507485.1:p.Arg1698Thr
ENST00000683159.1:c.576-552G>C
ENST00000683200.1:c.2441G>C	ENSP00000508052.1:p.Arg814Thr
ENST00000262189.11:c.5093G>C MANE Select	ENSP00000262189.6:p.Arg1698Thr
ENST00000360104.8:c.715G>C
ENST00000679645.1:c.*1186G>C	ENSP00000505745.1:n.*1186G>C
ENST00000679882.1:c.4868G>C	ENSP00000506154.1:p.Arg1623Thr
ENST00000680969.1:c.2489G>C	ENSP00000505951.1:p.Arg830Thr
ENST00000681033.1:c.3791G>C	ENSP00000505058.1:p.Arg1264Thr
ENST00000681755.1:n.18G>C
ENST00000262189.10:c.5093G>C	ENSP00000262189.6:p.Arg1698Thr
ENST00000355193.6:c.5093G>C	ENSP00000347325.3:p.Arg1698Thr
ENST00000473186.5:n.2804G>C
ENST00000558084.5:c.*2613G>C	ENSP00000453752.1:n.*2613G>C
NM_170606.2:c.5093G>C	NP_733751.2:p.Arg1698Thr
XM_005250025.3:c.5144G>C	XP_005250082.1:p.Arg1715Thr
XM_005250026.2:c.5141G>C	XP_005250083.1:p.Arg1714Thr
XM_005250027.3:c.5144G>C	XP_005250084.1:p.Arg1715Thr
XM_005250028.3:c.5144G>C	XP_005250085.1:p.Arg1715Thr
XM_005250031.3:c.5144G>C	XP_005250088.1:p.Arg1715Thr
XM_006716077.2:c.5144G>C	XP_006716140.1:p.Arg1715Thr
XM_006716078.2:c.5144G>C	XP_006716141.1:p.Arg1715Thr
XM_006716079.2:c.5144G>C	XP_006716142.1:p.Arg1715Thr
XM_011516450.1:c.5096G>C	XP_011514752.1:p.Arg1699Thr
XM_011516451.1:c.5024G>C	XP_011514753.1:p.Arg1675Thr
XM_011516452.1:c.4991G>C	XP_011514754.1:p.Arg1664Thr
XM_011516453.1:c.5144G>C	XP_011514755.1:p.Arg1715Thr
XM_011516454.1:c.4229G>C	XP_011514756.1:p.Arg1410Thr
XM_011516455.1:c.2690G>C	XP_011514757.1:p.Arg897Thr
XM_011516456.1:c.5096G>C	XP_011514758.1:p.Arg1699Thr
XR_428183.2:n.5352G>C
XM_005250025.4:c.5144G>C	XP_005250082.1:p.Arg1715Thr
XM_005250026.3:c.5141G>C	XP_005250083.1:p.Arg1714Thr
XM_005250027.4:c.5144G>C	XP_005250084.1:p.Arg1715Thr
XM_005250028.4:c.5144G>C	XP_005250085.1:p.Arg1715Thr
XM_005250031.4:c.5144G>C	XP_005250088.1:p.Arg1715Thr
XM_006716077.3:c.5144G>C	XP_006716140.1:p.Arg1715Thr
XM_006716078.3:c.5144G>C	XP_006716141.1:p.Arg1715Thr
XM_006716079.3:c.5144G>C	XP_006716142.1:p.Arg1715Thr
XM_011516450.2:c.5096G>C	XP_011514752.1:p.Arg1699Thr
XM_011516451.2:c.5024G>C	XP_011514753.1:p.Arg1675Thr
XM_011516452.2:c.4991G>C	XP_011514754.1:p.Arg1664Thr
XM_011516453.2:c.5144G>C	XP_011514755.1:p.Arg1715Thr
XM_011516454.2:c.4229G>C	XP_011514756.1:p.Arg1410Thr
XM_011516456.2:c.5096G>C	XP_011514758.1:p.Arg1699Thr
XM_017012480.1:c.5144G>C	XP_016867969.1:p.Arg1715Thr
XM_017012481.1:c.5141G>C	XP_016867970.1:p.Arg1714Thr
XM_017012482.1:c.5144G>C	XP_016867971.1:p.Arg1715Thr
XM_017012483.1:c.5144G>C	XP_016867972.1:p.Arg1715Thr
XM_017012484.1:c.5111G>C	XP_016867973.1:p.Arg1704Thr
XM_017012485.1:c.5093G>C	XP_016867974.1:p.Arg1698Thr
XM_017012486.1:c.5144G>C	XP_016867975.1:p.Arg1715Thr
XM_017012487.1:c.4997G>C	XP_016867976.1:p.Arg1666Thr
XM_017012488.1:c.5134-552G>C	XP_016867977.1:n.5134-552G>C
XM_017012489.1:c.1814G>C	XP_016867978.1:p.Arg605Thr
XM_017012490.2:c.1418G>C	XP_016867979.1:p.Arg473Thr
XM_024446852.1:c.5141G>C	XP_024302620.1:p.Arg1714Thr
XM_024446853.1:c.5144G>C	XP_024302621.1:p.Arg1715Thr
XR_428183.3:n.5376G>C
NM_170606.3:c.5093G>C MANE Select	NP_733751.2:p.Arg1698Thr