Canonical Allele Identifier: CA370093209

Gene: KMT2C

Linked Data

• MyVariant Identifiers: chr7:g.151845920A>C (hg19) ; chr7:g.152148835A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.152148835A>C , CM000669.2:g.152148835A>C	GRCh38
NC_000007.13:g.151845920A>C , CM000669.1:g.151845920A>C	GRCh37
NC_000007.12:g.151476853A>C	NCBI36
NG_033948.1:g.292171T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682040.1:c.1280T>G
ENST00000682116.1:n.2224T>G
ENST00000682283.1:c.13263T>G	ENSP00000507485.1:p.Ile4421Met
ENST00000682629.1:n.2392T>G
ENST00000683120.1:n.8284T>G
ENST00000683178.1:c.3665T>G
ENST00000683200.1:c.10602T>G	ENSP00000508052.1:p.Ile3534Met
ENST00000683337.1:n.4722T>G
ENST00000683502.1:c.3737T>G
ENST00000683621.1:n.1858T>G
ENST00000683640.1:n.1808T>G
ENST00000684069.1:c.1509T>G	ENSP00000507650.1:p.Ile503Met
ENST00000684261.1:c.7989T>G	ENSP00000508097.1:p.Ile2663Met
ENST00000684649.1:c.3737T>G
ENST00000262189.11:c.13092T>G MANE Select	ENSP00000262189.6:p.Ile4364Met
ENST00000360104.8:c.8879T>G
ENST00000418061.2:c.3734T>G
ENST00000424877.6:c.3668T>G
ENST00000679393.1:n.7803T>G
ENST00000679560.1:c.7992T>G	ENSP00000505094.1:p.Ile2664Met
ENST00000679882.1:c.12657T>G	ENSP00000506154.1:p.Ile4219Met
ENST00000680029.1:c.3669T>G
ENST00000680877.1:c.7992T>G	ENSP00000505724.1:p.Ile2664Met
ENST00000681923.1:n.2107T>G
ENST00000262189.10:c.13092T>G	ENSP00000262189.6:p.Ile4364Met
ENST00000355193.6:c.13092T>G	ENSP00000347325.3:p.Ile4364Met
ENST00000360104.7:c.5773T>G
ENST00000424877.5:c.2943T>G	ENSP00000410411.1:p.Ile981Met
ENST00000473186.5:n.10974T>G
ENST00000558084.5:c.*10612T>G	ENSP00000453752.1:n.*10612T>G
NM_170606.2:c.13092T>G	NP_733751.2:p.Ile4364Met
XM_005250025.3:c.13308T>G	XP_005250082.1:p.Ile4436Met
XM_005250026.2:c.13305T>G	XP_005250083.1:p.Ile4435Met
XM_005250027.3:c.13305T>G	XP_005250084.1:p.Ile4435Met
XM_005250028.3:c.13308T>G	XP_005250085.1:p.Ile4436Met
XM_005250031.3:c.13143T>G	XP_005250088.1:p.Ile4381Met
XM_006716077.2:c.13305T>G	XP_006716140.1:p.Ile4435Met
XM_006716078.2:c.13236T>G	XP_006716141.1:p.Ile4412Met
XM_006716079.2:c.13140T>G	XP_006716142.1:p.Ile4380Met
XM_011516450.1:c.13260T>G	XP_011514752.1:p.Ile4420Met
XM_011516451.1:c.13188T>G	XP_011514753.1:p.Ile4396Met
XM_011516452.1:c.13155T>G	XP_011514754.1:p.Ile4385Met
XM_011516453.1:c.13071T>G	XP_011514755.1:p.Ile4357Met
XM_011516454.1:c.12393T>G	XP_011514756.1:p.Ile4131Met
XM_011516455.1:c.10854T>G	XP_011514757.1:p.Ile3618Met
XM_011516456.1:c.13260T>G	XP_011514758.1:p.Ile4420Met
XM_005250025.4:c.13308T>G	XP_005250082.1:p.Ile4436Met
XM_005250026.3:c.13305T>G	XP_005250083.1:p.Ile4435Met
XM_005250027.4:c.13305T>G	XP_005250084.1:p.Ile4435Met
XM_005250028.4:c.13308T>G	XP_005250085.1:p.Ile4436Met
XM_005250031.4:c.13143T>G	XP_005250088.1:p.Ile4381Met
XM_006716077.3:c.13305T>G	XP_006716140.1:p.Ile4435Met
XM_006716078.3:c.13236T>G	XP_006716141.1:p.Ile4412Met
XM_006716079.3:c.13140T>G	XP_006716142.1:p.Ile4380Met
XM_011516450.2:c.13260T>G	XP_011514752.1:p.Ile4420Met
XM_011516451.2:c.13188T>G	XP_011514753.1:p.Ile4396Met
XM_011516452.2:c.13155T>G	XP_011514754.1:p.Ile4385Met
XM_011516453.2:c.13071T>G	XP_011514755.1:p.Ile4357Met
XM_011516454.2:c.12393T>G	XP_011514756.1:p.Ile4131Met
XM_011516456.2:c.13260T>G	XP_011514758.1:p.Ile4420Met
XM_017012480.1:c.13308T>G	XP_016867969.1:p.Ile4436Met
XM_017012481.1:c.13305T>G	XP_016867970.1:p.Ile4435Met
XM_017012482.1:c.13305T>G	XP_016867971.1:p.Ile4435Met
XM_017012483.1:c.13305T>G	XP_016867972.1:p.Ile4435Met
XM_017012484.1:c.13275T>G	XP_016867973.1:p.Ile4425Met
XM_017012485.1:c.13257T>G	XP_016867974.1:p.Ile4419Met
XM_017012486.1:c.13233T>G	XP_016867975.1:p.Ile4411Met
XM_017012487.1:c.13161T>G	XP_016867976.1:p.Ile4387Met
XM_017012488.1:c.13125T>G	XP_016867977.1:p.Ile4375Met
XM_017012489.1:c.9978T>G	XP_016867978.1:p.Ile3326Met
XM_017012490.2:c.9582T>G	XP_016867979.1:p.Ile3194Met
XM_024446852.1:c.13305T>G	XP_024302620.1:p.Ile4435Met
XM_024446853.1:c.13233T>G	XP_024302621.1:p.Ile4411Met
NM_170606.3:c.13092T>G MANE Select	NP_733751.2:p.Ile4364Met