Canonical Allele Identifier: CA370100541

Gene: KMT2C

Linked Data

• MyVariant Identifiers: chr7:g.151880230T>G (hg19) ; chr7:g.152183145T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.152183145T>G , CM000669.2:g.152183145T>G	GRCh38
NC_000007.13:g.151880230T>G , CM000669.1:g.151880230T>G	GRCh37
NC_000007.12:g.151511163T>G	NCBI36
NG_033948.1:g.257861A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000682176.1:c.1813A>C
ENST00000682283.1:c.5094A>C	ENSP00000507485.1:p.Arg1698Ser
ENST00000683159.1:c.576-551A>C
ENST00000683200.1:c.2442A>C	ENSP00000508052.1:p.Arg814Ser
ENST00000262189.11:c.5094A>C MANE Select	ENSP00000262189.6:p.Arg1698Ser
ENST00000360104.8:c.716A>C
ENST00000679645.1:c.*1187A>C	ENSP00000505745.1:n.*1187A>C
ENST00000679882.1:c.4869A>C	ENSP00000506154.1:p.Arg1623Ser
ENST00000680969.1:c.2490A>C	ENSP00000505951.1:p.Arg830Ser
ENST00000681033.1:c.3792A>C	ENSP00000505058.1:p.Arg1264Ser
ENST00000681755.1:n.19A>C
ENST00000262189.10:c.5094A>C	ENSP00000262189.6:p.Arg1698Ser
ENST00000355193.6:c.5094A>C	ENSP00000347325.3:p.Arg1698Ser
ENST00000473186.5:n.2805A>C
ENST00000558084.5:c.*2614A>C	ENSP00000453752.1:n.*2614A>C
NM_170606.2:c.5094A>C	NP_733751.2:p.Arg1698Ser
XM_005250025.3:c.5145A>C	XP_005250082.1:p.Arg1715Ser
XM_005250026.2:c.5142A>C	XP_005250083.1:p.Arg1714Ser
XM_005250027.3:c.5145A>C	XP_005250084.1:p.Arg1715Ser
XM_005250028.3:c.5145A>C	XP_005250085.1:p.Arg1715Ser
XM_005250031.3:c.5145A>C	XP_005250088.1:p.Arg1715Ser
XM_006716077.2:c.5145A>C	XP_006716140.1:p.Arg1715Ser
XM_006716078.2:c.5145A>C	XP_006716141.1:p.Arg1715Ser
XM_006716079.2:c.5145A>C	XP_006716142.1:p.Arg1715Ser
XM_011516450.1:c.5097A>C	XP_011514752.1:p.Arg1699Ser
XM_011516451.1:c.5025A>C	XP_011514753.1:p.Arg1675Ser
XM_011516452.1:c.4992A>C	XP_011514754.1:p.Arg1664Ser
XM_011516453.1:c.5145A>C	XP_011514755.1:p.Arg1715Ser
XM_011516454.1:c.4230A>C	XP_011514756.1:p.Arg1410Ser
XM_011516455.1:c.2691A>C	XP_011514757.1:p.Arg897Ser
XM_011516456.1:c.5097A>C	XP_011514758.1:p.Arg1699Ser
XR_428183.2:n.5353A>C
XM_005250025.4:c.5145A>C	XP_005250082.1:p.Arg1715Ser
XM_005250026.3:c.5142A>C	XP_005250083.1:p.Arg1714Ser
XM_005250027.4:c.5145A>C	XP_005250084.1:p.Arg1715Ser
XM_005250028.4:c.5145A>C	XP_005250085.1:p.Arg1715Ser
XM_005250031.4:c.5145A>C	XP_005250088.1:p.Arg1715Ser
XM_006716077.3:c.5145A>C	XP_006716140.1:p.Arg1715Ser
XM_006716078.3:c.5145A>C	XP_006716141.1:p.Arg1715Ser
XM_006716079.3:c.5145A>C	XP_006716142.1:p.Arg1715Ser
XM_011516450.2:c.5097A>C	XP_011514752.1:p.Arg1699Ser
XM_011516451.2:c.5025A>C	XP_011514753.1:p.Arg1675Ser
XM_011516452.2:c.4992A>C	XP_011514754.1:p.Arg1664Ser
XM_011516453.2:c.5145A>C	XP_011514755.1:p.Arg1715Ser
XM_011516454.2:c.4230A>C	XP_011514756.1:p.Arg1410Ser
XM_011516456.2:c.5097A>C	XP_011514758.1:p.Arg1699Ser
XM_017012480.1:c.5145A>C	XP_016867969.1:p.Arg1715Ser
XM_017012481.1:c.5142A>C	XP_016867970.1:p.Arg1714Ser
XM_017012482.1:c.5145A>C	XP_016867971.1:p.Arg1715Ser
XM_017012483.1:c.5145A>C	XP_016867972.1:p.Arg1715Ser
XM_017012484.1:c.5112A>C	XP_016867973.1:p.Arg1704Ser
XM_017012485.1:c.5094A>C	XP_016867974.1:p.Arg1698Ser
XM_017012486.1:c.5145A>C	XP_016867975.1:p.Arg1715Ser
XM_017012487.1:c.4998A>C	XP_016867976.1:p.Arg1666Ser
XM_017012488.1:c.5134-551A>C	XP_016867977.1:n.5134-551A>C
XM_017012489.1:c.1815A>C	XP_016867978.1:p.Arg605Ser
XM_017012490.2:c.1419A>C	XP_016867979.1:p.Arg473Ser
XM_024446852.1:c.5142A>C	XP_024302620.1:p.Arg1714Ser
XM_024446853.1:c.5145A>C	XP_024302621.1:p.Arg1715Ser
XR_428183.3:n.5377A>C
NM_170606.3:c.5094A>C MANE Select	NP_733751.2:p.Arg1698Ser