Canonical Allele Identifier: CA370093307

Gene: KMT2C

Linked Data

• MyVariant Identifiers: chr7:g.151845946T>G (hg19) ; chr7:g.152148861T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.152148861T>G , CM000669.2:g.152148861T>G	GRCh38
NC_000007.13:g.151845946T>G , CM000669.1:g.151845946T>G	GRCh37
NC_000007.12:g.151476879T>G	NCBI36
NG_033948.1:g.292145A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682040.1:c.1254A>C
ENST00000682116.1:n.2198A>C
ENST00000682283.1:c.13237A>C	ENSP00000507485.1:p.Lys4413Gln
ENST00000682629.1:n.2366A>C
ENST00000683120.1:n.8258A>C
ENST00000683178.1:c.3639A>C
ENST00000683200.1:c.10576A>C	ENSP00000508052.1:p.Lys3526Gln
ENST00000683337.1:n.4696A>C
ENST00000683502.1:c.3711A>C
ENST00000683621.1:n.1832A>C
ENST00000683640.1:n.1782A>C
ENST00000684069.1:c.1483A>C	ENSP00000507650.1:p.Lys495Gln
ENST00000684261.1:c.7963A>C	ENSP00000508097.1:p.Lys2655Gln
ENST00000684649.1:c.3711A>C
ENST00000262189.11:c.13066A>C MANE Select	ENSP00000262189.6:p.Lys4356Gln
ENST00000360104.8:c.8853A>C
ENST00000418061.2:c.3708A>C
ENST00000424877.6:c.3642A>C
ENST00000679393.1:n.7777A>C
ENST00000679560.1:c.7966A>C	ENSP00000505094.1:p.Lys2656Gln
ENST00000679882.1:c.12631A>C	ENSP00000506154.1:p.Lys4211Gln
ENST00000680029.1:c.3643A>C
ENST00000680877.1:c.7966A>C	ENSP00000505724.1:p.Lys2656Gln
ENST00000681923.1:n.2081A>C
ENST00000262189.10:c.13066A>C	ENSP00000262189.6:p.Lys4356Gln
ENST00000355193.6:c.13066A>C	ENSP00000347325.3:p.Lys4356Gln
ENST00000360104.7:c.5747A>C
ENST00000424877.5:c.2917A>C	ENSP00000410411.1:p.Lys973Gln
ENST00000473186.5:n.10948A>C
ENST00000558084.5:c.*10586A>C	ENSP00000453752.1:n.*10586A>C
NM_170606.2:c.13066A>C	NP_733751.2:p.Lys4356Gln
XM_005250025.3:c.13282A>C	XP_005250082.1:p.Lys4428Gln
XM_005250026.2:c.13279A>C	XP_005250083.1:p.Lys4427Gln
XM_005250027.3:c.13279A>C	XP_005250084.1:p.Lys4427Gln
XM_005250028.3:c.13282A>C	XP_005250085.1:p.Lys4428Gln
XM_005250031.3:c.13117A>C	XP_005250088.1:p.Lys4373Gln
XM_006716077.2:c.13279A>C	XP_006716140.1:p.Lys4427Gln
XM_006716078.2:c.13210A>C	XP_006716141.1:p.Lys4404Gln
XM_006716079.2:c.13114A>C	XP_006716142.1:p.Lys4372Gln
XM_011516450.1:c.13234A>C	XP_011514752.1:p.Lys4412Gln
XM_011516451.1:c.13162A>C	XP_011514753.1:p.Lys4388Gln
XM_011516452.1:c.13129A>C	XP_011514754.1:p.Lys4377Gln
XM_011516453.1:c.13045A>C	XP_011514755.1:p.Lys4349Gln
XM_011516454.1:c.12367A>C	XP_011514756.1:p.Lys4123Gln
XM_011516455.1:c.10828A>C	XP_011514757.1:p.Lys3610Gln
XM_011516456.1:c.13234A>C	XP_011514758.1:p.Lys4412Gln
XM_005250025.4:c.13282A>C	XP_005250082.1:p.Lys4428Gln
XM_005250026.3:c.13279A>C	XP_005250083.1:p.Lys4427Gln
XM_005250027.4:c.13279A>C	XP_005250084.1:p.Lys4427Gln
XM_005250028.4:c.13282A>C	XP_005250085.1:p.Lys4428Gln
XM_005250031.4:c.13117A>C	XP_005250088.1:p.Lys4373Gln
XM_006716077.3:c.13279A>C	XP_006716140.1:p.Lys4427Gln
XM_006716078.3:c.13210A>C	XP_006716141.1:p.Lys4404Gln
XM_006716079.3:c.13114A>C	XP_006716142.1:p.Lys4372Gln
XM_011516450.2:c.13234A>C	XP_011514752.1:p.Lys4412Gln
XM_011516451.2:c.13162A>C	XP_011514753.1:p.Lys4388Gln
XM_011516452.2:c.13129A>C	XP_011514754.1:p.Lys4377Gln
XM_011516453.2:c.13045A>C	XP_011514755.1:p.Lys4349Gln
XM_011516454.2:c.12367A>C	XP_011514756.1:p.Lys4123Gln
XM_011516456.2:c.13234A>C	XP_011514758.1:p.Lys4412Gln
XM_017012480.1:c.13282A>C	XP_016867969.1:p.Lys4428Gln
XM_017012481.1:c.13279A>C	XP_016867970.1:p.Lys4427Gln
XM_017012482.1:c.13279A>C	XP_016867971.1:p.Lys4427Gln
XM_017012483.1:c.13279A>C	XP_016867972.1:p.Lys4427Gln
XM_017012484.1:c.13249A>C	XP_016867973.1:p.Lys4417Gln
XM_017012485.1:c.13231A>C	XP_016867974.1:p.Lys4411Gln
XM_017012486.1:c.13207A>C	XP_016867975.1:p.Lys4403Gln
XM_017012487.1:c.13135A>C	XP_016867976.1:p.Lys4379Gln
XM_017012488.1:c.13099A>C	XP_016867977.1:p.Lys4367Gln
XM_017012489.1:c.9952A>C	XP_016867978.1:p.Lys3318Gln
XM_017012490.2:c.9556A>C	XP_016867979.1:p.Lys3186Gln
XM_024446852.1:c.13279A>C	XP_024302620.1:p.Lys4427Gln
XM_024446853.1:c.13207A>C	XP_024302621.1:p.Lys4403Gln
NM_170606.3:c.13066A>C MANE Select	NP_733751.2:p.Lys4356Gln