Canonical Allele Identifier: CA370093132

Gene: KMT2C

Linked Data

• MyVariant Identifiers: chr7:g.151845896T>G (hg19) ; chr7:g.152148811T>G (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682040.1:c.1304A>C
ENST00000682116.1:n.2248A>C
ENST00000682283.1:c.13287A>C	ENSP00000507485.1:p.Lys4429Asn
ENST00000682629.1:n.2416A>C
ENST00000683120.1:n.8308A>C
ENST00000683178.1:c.3689A>C
ENST00000683200.1:c.10626A>C	ENSP00000508052.1:p.Lys3542Asn
ENST00000683337.1:n.4746A>C
ENST00000683502.1:c.3761A>C
ENST00000683621.1:n.1882A>C
ENST00000683640.1:n.1832A>C
ENST00000684069.1:c.1533A>C	ENSP00000507650.1:p.Lys511Asn
ENST00000684261.1:c.8013A>C	ENSP00000508097.1:p.Lys2671Asn
ENST00000684649.1:c.3761A>C
ENST00000262189.11:c.13116A>C MANE Select	ENSP00000262189.6:p.Lys4372Asn
ENST00000360104.8:c.8903A>C
ENST00000418061.2:c.3758A>C
ENST00000424877.6:c.3692A>C
ENST00000679393.1:n.7827A>C
ENST00000679560.1:c.8016A>C	ENSP00000505094.1:p.Lys2672Asn
ENST00000679882.1:c.12681A>C	ENSP00000506154.1:p.Lys4227Asn
ENST00000680029.1:c.3693A>C
ENST00000680877.1:c.8016A>C	ENSP00000505724.1:p.Lys2672Asn
ENST00000681923.1:n.2131A>C
ENST00000262189.10:c.13116A>C	ENSP00000262189.6:p.Lys4372Asn
ENST00000355193.6:c.13116A>C	ENSP00000347325.3:p.Lys4372Asn
ENST00000360104.7:c.5797A>C
ENST00000424877.5:c.2967A>C	ENSP00000410411.1:p.Lys989Asn
ENST00000473186.5:n.10998A>C
ENST00000558084.5:c.*10636A>C	ENSP00000453752.1:n.*10636A>C
NM_170606.2:c.13116A>C	NP_733751.2:p.Lys4372Asn
XM_005250025.3:c.13332A>C	XP_005250082.1:p.Lys4444Asn
XM_005250026.2:c.13329A>C	XP_005250083.1:p.Lys4443Asn
XM_005250027.3:c.13329A>C	XP_005250084.1:p.Lys4443Asn
XM_005250028.3:c.13332A>C	XP_005250085.1:p.Lys4444Asn
XM_005250031.3:c.13167A>C	XP_005250088.1:p.Lys4389Asn
XM_006716077.2:c.13329A>C	XP_006716140.1:p.Lys4443Asn
XM_006716078.2:c.13260A>C	XP_006716141.1:p.Lys4420Asn
XM_006716079.2:c.13164A>C	XP_006716142.1:p.Lys4388Asn
XM_011516450.1:c.13284A>C	XP_011514752.1:p.Lys4428Asn
XM_011516451.1:c.13212A>C	XP_011514753.1:p.Lys4404Asn
XM_011516452.1:c.13179A>C	XP_011514754.1:p.Lys4393Asn
XM_011516453.1:c.13095A>C	XP_011514755.1:p.Lys4365Asn
XM_011516454.1:c.12417A>C	XP_011514756.1:p.Lys4139Asn
XM_011516455.1:c.10878A>C	XP_011514757.1:p.Lys3626Asn
XM_011516456.1:c.13284A>C	XP_011514758.1:p.Lys4428Asn
XM_005250025.4:c.13332A>C	XP_005250082.1:p.Lys4444Asn
XM_005250026.3:c.13329A>C	XP_005250083.1:p.Lys4443Asn
XM_005250027.4:c.13329A>C	XP_005250084.1:p.Lys4443Asn
XM_005250028.4:c.13332A>C	XP_005250085.1:p.Lys4444Asn
XM_005250031.4:c.13167A>C	XP_005250088.1:p.Lys4389Asn
XM_006716077.3:c.13329A>C	XP_006716140.1:p.Lys4443Asn
XM_006716078.3:c.13260A>C	XP_006716141.1:p.Lys4420Asn
XM_006716079.3:c.13164A>C	XP_006716142.1:p.Lys4388Asn
XM_011516450.2:c.13284A>C	XP_011514752.1:p.Lys4428Asn
XM_011516451.2:c.13212A>C	XP_011514753.1:p.Lys4404Asn
XM_011516452.2:c.13179A>C	XP_011514754.1:p.Lys4393Asn
XM_011516453.2:c.13095A>C	XP_011514755.1:p.Lys4365Asn
XM_011516454.2:c.12417A>C	XP_011514756.1:p.Lys4139Asn
XM_011516456.2:c.13284A>C	XP_011514758.1:p.Lys4428Asn
XM_017012480.1:c.13332A>C	XP_016867969.1:p.Lys4444Asn
XM_017012481.1:c.13329A>C	XP_016867970.1:p.Lys4443Asn
XM_017012482.1:c.13329A>C	XP_016867971.1:p.Lys4443Asn
XM_017012483.1:c.13329A>C	XP_016867972.1:p.Lys4443Asn
XM_017012484.1:c.13299A>C	XP_016867973.1:p.Lys4433Asn
XM_017012485.1:c.13281A>C	XP_016867974.1:p.Lys4427Asn
XM_017012486.1:c.13257A>C	XP_016867975.1:p.Lys4419Asn
XM_017012487.1:c.13185A>C	XP_016867976.1:p.Lys4395Asn
XM_017012488.1:c.13149A>C	XP_016867977.1:p.Lys4383Asn
XM_017012489.1:c.10002A>C	XP_016867978.1:p.Lys3334Asn
XM_017012490.2:c.9606A>C	XP_016867979.1:p.Lys3202Asn
XM_024446852.1:c.13329A>C	XP_024302620.1:p.Lys4443Asn
XM_024446853.1:c.13257A>C	XP_024302621.1:p.Lys4419Asn
NM_170606.3:c.13116A>C MANE Select	NP_733751.2:p.Lys4372Asn