Canonical Allele Identifier: CA370091920

Gene: KMT2C

Linked Data

• MyVariant Identifiers: chr7:g.151845782A>C (hg19) ; chr7:g.152148697A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.152148697A>C , CM000669.2:g.152148697A>C	GRCh38
NC_000007.13:g.151845782A>C , CM000669.1:g.151845782A>C	GRCh37
NC_000007.12:g.151476715A>C	NCBI36
NG_033948.1:g.292309T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682040.1:c.1418T>G
ENST00000682116.1:n.2362T>G
ENST00000682283.1:c.13401T>G	ENSP00000507485.1:p.Asp4467Glu
ENST00000682629.1:n.2530T>G
ENST00000683120.1:n.8422T>G
ENST00000683178.1:c.3803T>G
ENST00000683200.1:c.10740T>G	ENSP00000508052.1:p.Asp3580Glu
ENST00000683337.1:n.4860T>G
ENST00000683502.1:c.3875T>G
ENST00000683621.1:n.1996T>G
ENST00000683640.1:n.1946T>G
ENST00000684069.1:c.1647T>G	ENSP00000507650.1:p.Asp549Glu
ENST00000684261.1:c.8127T>G	ENSP00000508097.1:p.Asp2709Glu
ENST00000684649.1:c.3875T>G
ENST00000262189.11:c.13230T>G MANE Select	ENSP00000262189.6:p.Asp4410Glu
ENST00000360104.8:c.9017T>G
ENST00000418061.2:c.3872T>G
ENST00000424877.6:c.3806T>G
ENST00000679393.1:n.7941T>G
ENST00000679560.1:c.8130T>G	ENSP00000505094.1:p.Asp2710Glu
ENST00000679882.1:c.12795T>G	ENSP00000506154.1:p.Asp4265Glu
ENST00000680029.1:c.3807T>G
ENST00000680877.1:c.8130T>G	ENSP00000505724.1:p.Asp2710Glu
ENST00000681923.1:n.2245T>G
ENST00000262189.10:c.13230T>G	ENSP00000262189.6:p.Asp4410Glu
ENST00000355193.6:c.13230T>G	ENSP00000347325.3:p.Asp4410Glu
ENST00000360104.7:c.5911T>G
ENST00000424877.5:c.3081T>G	ENSP00000410411.1:p.Asp1027Glu
ENST00000473186.5:n.11112T>G
ENST00000558084.5:c.*10750T>G	ENSP00000453752.1:n.*10750T>G
NM_170606.2:c.13230T>G	NP_733751.2:p.Asp4410Glu
XM_005250025.3:c.13446T>G	XP_005250082.1:p.Asp4482Glu
XM_005250026.2:c.13443T>G	XP_005250083.1:p.Asp4481Glu
XM_005250027.3:c.13443T>G	XP_005250084.1:p.Asp4481Glu
XM_005250028.3:c.13446T>G	XP_005250085.1:p.Asp4482Glu
XM_005250031.3:c.13281T>G	XP_005250088.1:p.Asp4427Glu
XM_006716077.2:c.13443T>G	XP_006716140.1:p.Asp4481Glu
XM_006716078.2:c.13374T>G	XP_006716141.1:p.Asp4458Glu
XM_006716079.2:c.13278T>G	XP_006716142.1:p.Asp4426Glu
XM_011516450.1:c.13398T>G	XP_011514752.1:p.Asp4466Glu
XM_011516451.1:c.13326T>G	XP_011514753.1:p.Asp4442Glu
XM_011516452.1:c.13293T>G	XP_011514754.1:p.Asp4431Glu
XM_011516453.1:c.13209T>G	XP_011514755.1:p.Asp4403Glu
XM_011516454.1:c.12531T>G	XP_011514756.1:p.Asp4177Glu
XM_011516455.1:c.10992T>G	XP_011514757.1:p.Asp3664Glu
XM_011516456.1:c.13398T>G	XP_011514758.1:p.Asp4466Glu
XM_005250025.4:c.13446T>G	XP_005250082.1:p.Asp4482Glu
XM_005250026.3:c.13443T>G	XP_005250083.1:p.Asp4481Glu
XM_005250027.4:c.13443T>G	XP_005250084.1:p.Asp4481Glu
XM_005250028.4:c.13446T>G	XP_005250085.1:p.Asp4482Glu
XM_005250031.4:c.13281T>G	XP_005250088.1:p.Asp4427Glu
XM_006716077.3:c.13443T>G	XP_006716140.1:p.Asp4481Glu
XM_006716078.3:c.13374T>G	XP_006716141.1:p.Asp4458Glu
XM_006716079.3:c.13278T>G	XP_006716142.1:p.Asp4426Glu
XM_011516450.2:c.13398T>G	XP_011514752.1:p.Asp4466Glu
XM_011516451.2:c.13326T>G	XP_011514753.1:p.Asp4442Glu
XM_011516452.2:c.13293T>G	XP_011514754.1:p.Asp4431Glu
XM_011516453.2:c.13209T>G	XP_011514755.1:p.Asp4403Glu
XM_011516454.2:c.12531T>G	XP_011514756.1:p.Asp4177Glu
XM_011516456.2:c.13398T>G	XP_011514758.1:p.Asp4466Glu
XM_017012480.1:c.13446T>G	XP_016867969.1:p.Asp4482Glu
XM_017012481.1:c.13443T>G	XP_016867970.1:p.Asp4481Glu
XM_017012482.1:c.13443T>G	XP_016867971.1:p.Asp4481Glu
XM_017012483.1:c.13443T>G	XP_016867972.1:p.Asp4481Glu
XM_017012484.1:c.13413T>G	XP_016867973.1:p.Asp4471Glu
XM_017012485.1:c.13395T>G	XP_016867974.1:p.Asp4465Glu
XM_017012486.1:c.13371T>G	XP_016867975.1:p.Asp4457Glu
XM_017012487.1:c.13299T>G	XP_016867976.1:p.Asp4433Glu
XM_017012488.1:c.13263T>G	XP_016867977.1:p.Asp4421Glu
XM_017012489.1:c.10116T>G	XP_016867978.1:p.Asp3372Glu
XM_017012490.2:c.9720T>G	XP_016867979.1:p.Asp3240Glu
XM_024446852.1:c.13443T>G	XP_024302620.1:p.Asp4481Glu
XM_024446853.1:c.13371T>G	XP_024302621.1:p.Asp4457Glu
NM_170606.3:c.13230T>G MANE Select	NP_733751.2:p.Asp4410Glu