Canonical Allele Identifier: CA370093191

Gene: KMT2C

Linked Data

• MyVariant Identifiers: chr7:g.151845914G>C (hg19) ; chr7:g.152148829G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.152148829G>C , CM000669.2:g.152148829G>C	GRCh38
NC_000007.13:g.151845914G>C , CM000669.1:g.151845914G>C	GRCh37
NC_000007.12:g.151476847G>C	NCBI36
NG_033948.1:g.292177C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682040.1:c.1286C>G
ENST00000682116.1:n.2230C>G
ENST00000682283.1:c.13269C>G	ENSP00000507485.1:p.Ile4423Met
ENST00000682629.1:n.2398C>G
ENST00000683120.1:n.8290C>G
ENST00000683178.1:c.3671C>G
ENST00000683200.1:c.10608C>G	ENSP00000508052.1:p.Ile3536Met
ENST00000683337.1:n.4728C>G
ENST00000683502.1:c.3743C>G
ENST00000683621.1:n.1864C>G
ENST00000683640.1:n.1814C>G
ENST00000684069.1:c.1515C>G	ENSP00000507650.1:p.Ile505Met
ENST00000684261.1:c.7995C>G	ENSP00000508097.1:p.Ile2665Met
ENST00000684649.1:c.3743C>G
ENST00000262189.11:c.13098C>G MANE Select	ENSP00000262189.6:p.Ile4366Met
ENST00000360104.8:c.8885C>G
ENST00000418061.2:c.3740C>G
ENST00000424877.6:c.3674C>G
ENST00000679393.1:n.7809C>G
ENST00000679560.1:c.7998C>G	ENSP00000505094.1:p.Ile2666Met
ENST00000679882.1:c.12663C>G	ENSP00000506154.1:p.Ile4221Met
ENST00000680029.1:c.3675C>G
ENST00000680877.1:c.7998C>G	ENSP00000505724.1:p.Ile2666Met
ENST00000681923.1:n.2113C>G
ENST00000262189.10:c.13098C>G	ENSP00000262189.6:p.Ile4366Met
ENST00000355193.6:c.13098C>G	ENSP00000347325.3:p.Ile4366Met
ENST00000360104.7:c.5779C>G
ENST00000424877.5:c.2949C>G	ENSP00000410411.1:p.Ile983Met
ENST00000473186.5:n.10980C>G
ENST00000558084.5:c.*10618C>G	ENSP00000453752.1:n.*10618C>G
NM_170606.2:c.13098C>G	NP_733751.2:p.Ile4366Met
XM_005250025.3:c.13314C>G	XP_005250082.1:p.Ile4438Met
XM_005250026.2:c.13311C>G	XP_005250083.1:p.Ile4437Met
XM_005250027.3:c.13311C>G	XP_005250084.1:p.Ile4437Met
XM_005250028.3:c.13314C>G	XP_005250085.1:p.Ile4438Met
XM_005250031.3:c.13149C>G	XP_005250088.1:p.Ile4383Met
XM_006716077.2:c.13311C>G	XP_006716140.1:p.Ile4437Met
XM_006716078.2:c.13242C>G	XP_006716141.1:p.Ile4414Met
XM_006716079.2:c.13146C>G	XP_006716142.1:p.Ile4382Met
XM_011516450.1:c.13266C>G	XP_011514752.1:p.Ile4422Met
XM_011516451.1:c.13194C>G	XP_011514753.1:p.Ile4398Met
XM_011516452.1:c.13161C>G	XP_011514754.1:p.Ile4387Met
XM_011516453.1:c.13077C>G	XP_011514755.1:p.Ile4359Met
XM_011516454.1:c.12399C>G	XP_011514756.1:p.Ile4133Met
XM_011516455.1:c.10860C>G	XP_011514757.1:p.Ile3620Met
XM_011516456.1:c.13266C>G	XP_011514758.1:p.Ile4422Met
XM_005250025.4:c.13314C>G	XP_005250082.1:p.Ile4438Met
XM_005250026.3:c.13311C>G	XP_005250083.1:p.Ile4437Met
XM_005250027.4:c.13311C>G	XP_005250084.1:p.Ile4437Met
XM_005250028.4:c.13314C>G	XP_005250085.1:p.Ile4438Met
XM_005250031.4:c.13149C>G	XP_005250088.1:p.Ile4383Met
XM_006716077.3:c.13311C>G	XP_006716140.1:p.Ile4437Met
XM_006716078.3:c.13242C>G	XP_006716141.1:p.Ile4414Met
XM_006716079.3:c.13146C>G	XP_006716142.1:p.Ile4382Met
XM_011516450.2:c.13266C>G	XP_011514752.1:p.Ile4422Met
XM_011516451.2:c.13194C>G	XP_011514753.1:p.Ile4398Met
XM_011516452.2:c.13161C>G	XP_011514754.1:p.Ile4387Met
XM_011516453.2:c.13077C>G	XP_011514755.1:p.Ile4359Met
XM_011516454.2:c.12399C>G	XP_011514756.1:p.Ile4133Met
XM_011516456.2:c.13266C>G	XP_011514758.1:p.Ile4422Met
XM_017012480.1:c.13314C>G	XP_016867969.1:p.Ile4438Met
XM_017012481.1:c.13311C>G	XP_016867970.1:p.Ile4437Met
XM_017012482.1:c.13311C>G	XP_016867971.1:p.Ile4437Met
XM_017012483.1:c.13311C>G	XP_016867972.1:p.Ile4437Met
XM_017012484.1:c.13281C>G	XP_016867973.1:p.Ile4427Met
XM_017012485.1:c.13263C>G	XP_016867974.1:p.Ile4421Met
XM_017012486.1:c.13239C>G	XP_016867975.1:p.Ile4413Met
XM_017012487.1:c.13167C>G	XP_016867976.1:p.Ile4389Met
XM_017012488.1:c.13131C>G	XP_016867977.1:p.Ile4377Met
XM_017012489.1:c.9984C>G	XP_016867978.1:p.Ile3328Met
XM_017012490.2:c.9588C>G	XP_016867979.1:p.Ile3196Met
XM_024446852.1:c.13311C>G	XP_024302620.1:p.Ile4437Met
XM_024446853.1:c.13239C>G	XP_024302621.1:p.Ile4413Met
NM_170606.3:c.13098C>G MANE Select	NP_733751.2:p.Ile4366Met