Canonical Allele Identifier: CA458884942

Gene: KMT2C

Linked Data

• MyVariant Identifiers: chr7:g.151845962T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.152148877T>C , CM000669.2:g.152148877T>C	GRCh38
NC_000007.13:g.151845962T>C , CM000669.1:g.151845962T>C	GRCh37
NC_000007.12:g.151476895T>C	NCBI36
NG_033948.1:g.292129A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682040.1:c.1238A>G
ENST00000682116.1:n.2182A>G
ENST00000682283.1:c.13221A>G	ENSP00000507485.1:p.Lys4407=
ENST00000682629.1:n.2350A>G
ENST00000683120.1:n.8242A>G
ENST00000683178.1:c.3623A>G
ENST00000683200.1:c.10560A>G	ENSP00000508052.1:p.Lys3520=
ENST00000683337.1:n.4680A>G
ENST00000683502.1:c.3695A>G
ENST00000683621.1:n.1816A>G
ENST00000683640.1:n.1766A>G
ENST00000684069.1:c.1467A>G	ENSP00000507650.1:p.Lys489=
ENST00000684261.1:c.7947A>G	ENSP00000508097.1:p.Lys2649=
ENST00000684649.1:c.3695A>G
ENST00000262189.11:c.13050A>G MANE Select	ENSP00000262189.6:p.Lys4350=
ENST00000360104.8:c.8837A>G
ENST00000418061.2:c.3692A>G
ENST00000424877.6:c.3626A>G
ENST00000679393.1:n.7761A>G
ENST00000679560.1:c.7950A>G	ENSP00000505094.1:p.Lys2650=
ENST00000679882.1:c.12615A>G	ENSP00000506154.1:p.Lys4205=
ENST00000680029.1:c.3627A>G
ENST00000680877.1:c.7950A>G	ENSP00000505724.1:p.Lys2650=
ENST00000681923.1:n.2065A>G
ENST00000262189.10:c.13050A>G	ENSP00000262189.6:p.Lys4350=
ENST00000355193.6:c.13050A>G	ENSP00000347325.3:p.Lys4350=
ENST00000360104.7:c.5731A>G
ENST00000424877.5:c.2901A>G	ENSP00000410411.1:p.Lys967=
ENST00000473186.5:n.10932A>G
ENST00000558084.5:c.*10570A>G	ENSP00000453752.1:n.*10570A>G
NM_170606.2:c.13050A>G	NP_733751.2:p.Lys4350=
XM_005250025.3:c.13266A>G	XP_005250082.1:p.Lys4422=
XM_005250026.2:c.13263A>G	XP_005250083.1:p.Lys4421=
XM_005250027.3:c.13263A>G	XP_005250084.1:p.Lys4421=
XM_005250028.3:c.13266A>G	XP_005250085.1:p.Lys4422=
XM_005250031.3:c.13101A>G	XP_005250088.1:p.Lys4367=
XM_006716077.2:c.13263A>G	XP_006716140.1:p.Lys4421=
XM_006716078.2:c.13194A>G	XP_006716141.1:p.Lys4398=
XM_006716079.2:c.13098A>G	XP_006716142.1:p.Lys4366=
XM_011516450.1:c.13218A>G	XP_011514752.1:p.Lys4406=
XM_011516451.1:c.13146A>G	XP_011514753.1:p.Lys4382=
XM_011516452.1:c.13113A>G	XP_011514754.1:p.Lys4371=
XM_011516453.1:c.13029A>G	XP_011514755.1:p.Lys4343=
XM_011516454.1:c.12351A>G	XP_011514756.1:p.Lys4117=
XM_011516455.1:c.10812A>G	XP_011514757.1:p.Lys3604=
XM_011516456.1:c.13218A>G	XP_011514758.1:p.Lys4406=
XM_005250025.4:c.13266A>G	XP_005250082.1:p.Lys4422=
XM_005250026.3:c.13263A>G	XP_005250083.1:p.Lys4421=
XM_005250027.4:c.13263A>G	XP_005250084.1:p.Lys4421=
XM_005250028.4:c.13266A>G	XP_005250085.1:p.Lys4422=
XM_005250031.4:c.13101A>G	XP_005250088.1:p.Lys4367=
XM_006716077.3:c.13263A>G	XP_006716140.1:p.Lys4421=
XM_006716078.3:c.13194A>G	XP_006716141.1:p.Lys4398=
XM_006716079.3:c.13098A>G	XP_006716142.1:p.Lys4366=
XM_011516450.2:c.13218A>G	XP_011514752.1:p.Lys4406=
XM_011516451.2:c.13146A>G	XP_011514753.1:p.Lys4382=
XM_011516452.2:c.13113A>G	XP_011514754.1:p.Lys4371=
XM_011516453.2:c.13029A>G	XP_011514755.1:p.Lys4343=
XM_011516454.2:c.12351A>G	XP_011514756.1:p.Lys4117=
XM_011516456.2:c.13218A>G	XP_011514758.1:p.Lys4406=
XM_017012480.1:c.13266A>G	XP_016867969.1:p.Lys4422=
XM_017012481.1:c.13263A>G	XP_016867970.1:p.Lys4421=
XM_017012482.1:c.13263A>G	XP_016867971.1:p.Lys4421=
XM_017012483.1:c.13263A>G	XP_016867972.1:p.Lys4421=
XM_017012484.1:c.13233A>G	XP_016867973.1:p.Lys4411=
XM_017012485.1:c.13215A>G	XP_016867974.1:p.Lys4405=
XM_017012486.1:c.13191A>G	XP_016867975.1:p.Lys4397=
XM_017012487.1:c.13119A>G	XP_016867976.1:p.Lys4373=
XM_017012488.1:c.13083A>G	XP_016867977.1:p.Lys4361=
XM_017012489.1:c.9936A>G	XP_016867978.1:p.Lys3312=
XM_017012490.2:c.9540A>G	XP_016867979.1:p.Lys3180=
XM_024446852.1:c.13263A>G	XP_024302620.1:p.Lys4421=
XM_024446853.1:c.13191A>G	XP_024302621.1:p.Lys4397=
NM_170606.3:c.13050A>G MANE Select	NP_733751.2:p.Lys4350=