Canonical Allele Identifier: CA458884783

Gene: KMT2C

Linked Data

• MyVariant Identifiers: chr7:g.151845902T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.152148817T>C , CM000669.2:g.152148817T>C	GRCh38
NC_000007.13:g.151845902T>C , CM000669.1:g.151845902T>C	GRCh37
NC_000007.12:g.151476835T>C	NCBI36
NG_033948.1:g.292189A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682040.1:c.1298A>G
ENST00000682116.1:n.2242A>G
ENST00000682283.1:c.13281A>G	ENSP00000507485.1:p.Thr4427=
ENST00000682629.1:n.2410A>G
ENST00000683120.1:n.8302A>G
ENST00000683178.1:c.3683A>G
ENST00000683200.1:c.10620A>G	ENSP00000508052.1:p.Thr3540=
ENST00000683337.1:n.4740A>G
ENST00000683502.1:c.3755A>G
ENST00000683621.1:n.1876A>G
ENST00000683640.1:n.1826A>G
ENST00000684069.1:c.1527A>G	ENSP00000507650.1:p.Thr509=
ENST00000684261.1:c.8007A>G	ENSP00000508097.1:p.Thr2669=
ENST00000684649.1:c.3755A>G
ENST00000262189.11:c.13110A>G MANE Select	ENSP00000262189.6:p.Thr4370=
ENST00000360104.8:c.8897A>G
ENST00000418061.2:c.3752A>G
ENST00000424877.6:c.3686A>G
ENST00000679393.1:n.7821A>G
ENST00000679560.1:c.8010A>G	ENSP00000505094.1:p.Thr2670=
ENST00000679882.1:c.12675A>G	ENSP00000506154.1:p.Thr4225=
ENST00000680029.1:c.3687A>G
ENST00000680877.1:c.8010A>G	ENSP00000505724.1:p.Thr2670=
ENST00000681923.1:n.2125A>G
ENST00000262189.10:c.13110A>G	ENSP00000262189.6:p.Thr4370=
ENST00000355193.6:c.13110A>G	ENSP00000347325.3:p.Thr4370=
ENST00000360104.7:c.5791A>G
ENST00000424877.5:c.2961A>G	ENSP00000410411.1:p.Thr987=
ENST00000473186.5:n.10992A>G
ENST00000558084.5:c.*10630A>G	ENSP00000453752.1:n.*10630A>G
NM_170606.2:c.13110A>G	NP_733751.2:p.Thr4370=
XM_005250025.3:c.13326A>G	XP_005250082.1:p.Thr4442=
XM_005250026.2:c.13323A>G	XP_005250083.1:p.Thr4441=
XM_005250027.3:c.13323A>G	XP_005250084.1:p.Thr4441=
XM_005250028.3:c.13326A>G	XP_005250085.1:p.Thr4442=
XM_005250031.3:c.13161A>G	XP_005250088.1:p.Thr4387=
XM_006716077.2:c.13323A>G	XP_006716140.1:p.Thr4441=
XM_006716078.2:c.13254A>G	XP_006716141.1:p.Thr4418=
XM_006716079.2:c.13158A>G	XP_006716142.1:p.Thr4386=
XM_011516450.1:c.13278A>G	XP_011514752.1:p.Thr4426=
XM_011516451.1:c.13206A>G	XP_011514753.1:p.Thr4402=
XM_011516452.1:c.13173A>G	XP_011514754.1:p.Thr4391=
XM_011516453.1:c.13089A>G	XP_011514755.1:p.Thr4363=
XM_011516454.1:c.12411A>G	XP_011514756.1:p.Thr4137=
XM_011516455.1:c.10872A>G	XP_011514757.1:p.Thr3624=
XM_011516456.1:c.13278A>G	XP_011514758.1:p.Thr4426=
XM_005250025.4:c.13326A>G	XP_005250082.1:p.Thr4442=
XM_005250026.3:c.13323A>G	XP_005250083.1:p.Thr4441=
XM_005250027.4:c.13323A>G	XP_005250084.1:p.Thr4441=
XM_005250028.4:c.13326A>G	XP_005250085.1:p.Thr4442=
XM_005250031.4:c.13161A>G	XP_005250088.1:p.Thr4387=
XM_006716077.3:c.13323A>G	XP_006716140.1:p.Thr4441=
XM_006716078.3:c.13254A>G	XP_006716141.1:p.Thr4418=
XM_006716079.3:c.13158A>G	XP_006716142.1:p.Thr4386=
XM_011516450.2:c.13278A>G	XP_011514752.1:p.Thr4426=
XM_011516451.2:c.13206A>G	XP_011514753.1:p.Thr4402=
XM_011516452.2:c.13173A>G	XP_011514754.1:p.Thr4391=
XM_011516453.2:c.13089A>G	XP_011514755.1:p.Thr4363=
XM_011516454.2:c.12411A>G	XP_011514756.1:p.Thr4137=
XM_011516456.2:c.13278A>G	XP_011514758.1:p.Thr4426=
XM_017012480.1:c.13326A>G	XP_016867969.1:p.Thr4442=
XM_017012481.1:c.13323A>G	XP_016867970.1:p.Thr4441=
XM_017012482.1:c.13323A>G	XP_016867971.1:p.Thr4441=
XM_017012483.1:c.13323A>G	XP_016867972.1:p.Thr4441=
XM_017012484.1:c.13293A>G	XP_016867973.1:p.Thr4431=
XM_017012485.1:c.13275A>G	XP_016867974.1:p.Thr4425=
XM_017012486.1:c.13251A>G	XP_016867975.1:p.Thr4417=
XM_017012487.1:c.13179A>G	XP_016867976.1:p.Thr4393=
XM_017012488.1:c.13143A>G	XP_016867977.1:p.Thr4381=
XM_017012489.1:c.9996A>G	XP_016867978.1:p.Thr3332=
XM_017012490.2:c.9600A>G	XP_016867979.1:p.Thr3200=
XM_024446852.1:c.13323A>G	XP_024302620.1:p.Thr4441=
XM_024446853.1:c.13251A>G	XP_024302621.1:p.Thr4417=
NM_170606.3:c.13110A>G MANE Select	NP_733751.2:p.Thr4370=