Canonical Allele Identifier: CA458884767

Gene: KMT2C

Linked Data

• MyVariant Identifiers: chr7:g.151845896T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.152148811T>C , CM000669.2:g.152148811T>C	GRCh38
NC_000007.13:g.151845896T>C , CM000669.1:g.151845896T>C	GRCh37
NC_000007.12:g.151476829T>C	NCBI36
NG_033948.1:g.292195A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682040.1:c.1304A>G
ENST00000682116.1:n.2248A>G
ENST00000682283.1:c.13287A>G	ENSP00000507485.1:p.Lys4429=
ENST00000682629.1:n.2416A>G
ENST00000683120.1:n.8308A>G
ENST00000683178.1:c.3689A>G
ENST00000683200.1:c.10626A>G	ENSP00000508052.1:p.Lys3542=
ENST00000683337.1:n.4746A>G
ENST00000683502.1:c.3761A>G
ENST00000683621.1:n.1882A>G
ENST00000683640.1:n.1832A>G
ENST00000684069.1:c.1533A>G	ENSP00000507650.1:p.Lys511=
ENST00000684261.1:c.8013A>G	ENSP00000508097.1:p.Lys2671=
ENST00000684649.1:c.3761A>G
ENST00000262189.11:c.13116A>G MANE Select	ENSP00000262189.6:p.Lys4372=
ENST00000360104.8:c.8903A>G
ENST00000418061.2:c.3758A>G
ENST00000424877.6:c.3692A>G
ENST00000679393.1:n.7827A>G
ENST00000679560.1:c.8016A>G	ENSP00000505094.1:p.Lys2672=
ENST00000679882.1:c.12681A>G	ENSP00000506154.1:p.Lys4227=
ENST00000680029.1:c.3693A>G
ENST00000680877.1:c.8016A>G	ENSP00000505724.1:p.Lys2672=
ENST00000681923.1:n.2131A>G
ENST00000262189.10:c.13116A>G	ENSP00000262189.6:p.Lys4372=
ENST00000355193.6:c.13116A>G	ENSP00000347325.3:p.Lys4372=
ENST00000360104.7:c.5797A>G
ENST00000424877.5:c.2967A>G	ENSP00000410411.1:p.Lys989=
ENST00000473186.5:n.10998A>G
ENST00000558084.5:c.*10636A>G	ENSP00000453752.1:n.*10636A>G
NM_170606.2:c.13116A>G	NP_733751.2:p.Lys4372=
XM_005250025.3:c.13332A>G	XP_005250082.1:p.Lys4444=
XM_005250026.2:c.13329A>G	XP_005250083.1:p.Lys4443=
XM_005250027.3:c.13329A>G	XP_005250084.1:p.Lys4443=
XM_005250028.3:c.13332A>G	XP_005250085.1:p.Lys4444=
XM_005250031.3:c.13167A>G	XP_005250088.1:p.Lys4389=
XM_006716077.2:c.13329A>G	XP_006716140.1:p.Lys4443=
XM_006716078.2:c.13260A>G	XP_006716141.1:p.Lys4420=
XM_006716079.2:c.13164A>G	XP_006716142.1:p.Lys4388=
XM_011516450.1:c.13284A>G	XP_011514752.1:p.Lys4428=
XM_011516451.1:c.13212A>G	XP_011514753.1:p.Lys4404=
XM_011516452.1:c.13179A>G	XP_011514754.1:p.Lys4393=
XM_011516453.1:c.13095A>G	XP_011514755.1:p.Lys4365=
XM_011516454.1:c.12417A>G	XP_011514756.1:p.Lys4139=
XM_011516455.1:c.10878A>G	XP_011514757.1:p.Lys3626=
XM_011516456.1:c.13284A>G	XP_011514758.1:p.Lys4428=
XM_005250025.4:c.13332A>G	XP_005250082.1:p.Lys4444=
XM_005250026.3:c.13329A>G	XP_005250083.1:p.Lys4443=
XM_005250027.4:c.13329A>G	XP_005250084.1:p.Lys4443=
XM_005250028.4:c.13332A>G	XP_005250085.1:p.Lys4444=
XM_005250031.4:c.13167A>G	XP_005250088.1:p.Lys4389=
XM_006716077.3:c.13329A>G	XP_006716140.1:p.Lys4443=
XM_006716078.3:c.13260A>G	XP_006716141.1:p.Lys4420=
XM_006716079.3:c.13164A>G	XP_006716142.1:p.Lys4388=
XM_011516450.2:c.13284A>G	XP_011514752.1:p.Lys4428=
XM_011516451.2:c.13212A>G	XP_011514753.1:p.Lys4404=
XM_011516452.2:c.13179A>G	XP_011514754.1:p.Lys4393=
XM_011516453.2:c.13095A>G	XP_011514755.1:p.Lys4365=
XM_011516454.2:c.12417A>G	XP_011514756.1:p.Lys4139=
XM_011516456.2:c.13284A>G	XP_011514758.1:p.Lys4428=
XM_017012480.1:c.13332A>G	XP_016867969.1:p.Lys4444=
XM_017012481.1:c.13329A>G	XP_016867970.1:p.Lys4443=
XM_017012482.1:c.13329A>G	XP_016867971.1:p.Lys4443=
XM_017012483.1:c.13329A>G	XP_016867972.1:p.Lys4443=
XM_017012484.1:c.13299A>G	XP_016867973.1:p.Lys4433=
XM_017012485.1:c.13281A>G	XP_016867974.1:p.Lys4427=
XM_017012486.1:c.13257A>G	XP_016867975.1:p.Lys4419=
XM_017012487.1:c.13185A>G	XP_016867976.1:p.Lys4395=
XM_017012488.1:c.13149A>G	XP_016867977.1:p.Lys4383=
XM_017012489.1:c.10002A>G	XP_016867978.1:p.Lys3334=
XM_017012490.2:c.9606A>G	XP_016867979.1:p.Lys3202=
XM_024446852.1:c.13329A>G	XP_024302620.1:p.Lys4443=
XM_024446853.1:c.13257A>G	XP_024302621.1:p.Lys4419=
NM_170606.3:c.13116A>G MANE Select	NP_733751.2:p.Lys4372=