Canonical Allele Identifier: CA370093301

Gene: KMT2C

Linked Data

• MyVariant Identifiers: chr7:g.151845945T>C (hg19) ; chr7:g.152148860T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.152148860T>C , CM000669.2:g.152148860T>C	GRCh38
NC_000007.13:g.151845945T>C , CM000669.1:g.151845945T>C	GRCh37
NC_000007.12:g.151476878T>C	NCBI36
NG_033948.1:g.292146A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682040.1:c.1255A>G
ENST00000682116.1:n.2199A>G
ENST00000682283.1:c.13238A>G	ENSP00000507485.1:p.Lys4413Arg
ENST00000682629.1:n.2367A>G
ENST00000683120.1:n.8259A>G
ENST00000683178.1:c.3640A>G
ENST00000683200.1:c.10577A>G	ENSP00000508052.1:p.Lys3526Arg
ENST00000683337.1:n.4697A>G
ENST00000683502.1:c.3712A>G
ENST00000683621.1:n.1833A>G
ENST00000683640.1:n.1783A>G
ENST00000684069.1:c.1484A>G	ENSP00000507650.1:p.Lys495Arg
ENST00000684261.1:c.7964A>G	ENSP00000508097.1:p.Lys2655Arg
ENST00000684649.1:c.3712A>G
ENST00000262189.11:c.13067A>G MANE Select	ENSP00000262189.6:p.Lys4356Arg
ENST00000360104.8:c.8854A>G
ENST00000418061.2:c.3709A>G
ENST00000424877.6:c.3643A>G
ENST00000679393.1:n.7778A>G
ENST00000679560.1:c.7967A>G	ENSP00000505094.1:p.Lys2656Arg
ENST00000679882.1:c.12632A>G	ENSP00000506154.1:p.Lys4211Arg
ENST00000680029.1:c.3644A>G
ENST00000680877.1:c.7967A>G	ENSP00000505724.1:p.Lys2656Arg
ENST00000681923.1:n.2082A>G
ENST00000262189.10:c.13067A>G	ENSP00000262189.6:p.Lys4356Arg
ENST00000355193.6:c.13067A>G	ENSP00000347325.3:p.Lys4356Arg
ENST00000360104.7:c.5748A>G
ENST00000424877.5:c.2918A>G	ENSP00000410411.1:p.Lys973Arg
ENST00000473186.5:n.10949A>G
ENST00000558084.5:c.*10587A>G	ENSP00000453752.1:n.*10587A>G
NM_170606.2:c.13067A>G	NP_733751.2:p.Lys4356Arg
XM_005250025.3:c.13283A>G	XP_005250082.1:p.Lys4428Arg
XM_005250026.2:c.13280A>G	XP_005250083.1:p.Lys4427Arg
XM_005250027.3:c.13280A>G	XP_005250084.1:p.Lys4427Arg
XM_005250028.3:c.13283A>G	XP_005250085.1:p.Lys4428Arg
XM_005250031.3:c.13118A>G	XP_005250088.1:p.Lys4373Arg
XM_006716077.2:c.13280A>G	XP_006716140.1:p.Lys4427Arg
XM_006716078.2:c.13211A>G	XP_006716141.1:p.Lys4404Arg
XM_006716079.2:c.13115A>G	XP_006716142.1:p.Lys4372Arg
XM_011516450.1:c.13235A>G	XP_011514752.1:p.Lys4412Arg
XM_011516451.1:c.13163A>G	XP_011514753.1:p.Lys4388Arg
XM_011516452.1:c.13130A>G	XP_011514754.1:p.Lys4377Arg
XM_011516453.1:c.13046A>G	XP_011514755.1:p.Lys4349Arg
XM_011516454.1:c.12368A>G	XP_011514756.1:p.Lys4123Arg
XM_011516455.1:c.10829A>G	XP_011514757.1:p.Lys3610Arg
XM_011516456.1:c.13235A>G	XP_011514758.1:p.Lys4412Arg
XM_005250025.4:c.13283A>G	XP_005250082.1:p.Lys4428Arg
XM_005250026.3:c.13280A>G	XP_005250083.1:p.Lys4427Arg
XM_005250027.4:c.13280A>G	XP_005250084.1:p.Lys4427Arg
XM_005250028.4:c.13283A>G	XP_005250085.1:p.Lys4428Arg
XM_005250031.4:c.13118A>G	XP_005250088.1:p.Lys4373Arg
XM_006716077.3:c.13280A>G	XP_006716140.1:p.Lys4427Arg
XM_006716078.3:c.13211A>G	XP_006716141.1:p.Lys4404Arg
XM_006716079.3:c.13115A>G	XP_006716142.1:p.Lys4372Arg
XM_011516450.2:c.13235A>G	XP_011514752.1:p.Lys4412Arg
XM_011516451.2:c.13163A>G	XP_011514753.1:p.Lys4388Arg
XM_011516452.2:c.13130A>G	XP_011514754.1:p.Lys4377Arg
XM_011516453.2:c.13046A>G	XP_011514755.1:p.Lys4349Arg
XM_011516454.2:c.12368A>G	XP_011514756.1:p.Lys4123Arg
XM_011516456.2:c.13235A>G	XP_011514758.1:p.Lys4412Arg
XM_017012480.1:c.13283A>G	XP_016867969.1:p.Lys4428Arg
XM_017012481.1:c.13280A>G	XP_016867970.1:p.Lys4427Arg
XM_017012482.1:c.13280A>G	XP_016867971.1:p.Lys4427Arg
XM_017012483.1:c.13280A>G	XP_016867972.1:p.Lys4427Arg
XM_017012484.1:c.13250A>G	XP_016867973.1:p.Lys4417Arg
XM_017012485.1:c.13232A>G	XP_016867974.1:p.Lys4411Arg
XM_017012486.1:c.13208A>G	XP_016867975.1:p.Lys4403Arg
XM_017012487.1:c.13136A>G	XP_016867976.1:p.Lys4379Arg
XM_017012488.1:c.13100A>G	XP_016867977.1:p.Lys4367Arg
XM_017012489.1:c.9953A>G	XP_016867978.1:p.Lys3318Arg
XM_017012490.2:c.9557A>G	XP_016867979.1:p.Lys3186Arg
XM_024446852.1:c.13280A>G	XP_024302620.1:p.Lys4427Arg
XM_024446853.1:c.13208A>G	XP_024302621.1:p.Lys4403Arg
NM_170606.3:c.13067A>G MANE Select	NP_733751.2:p.Lys4356Arg