Canonical Allele Identifier: CA370093267

Gene: KMT2C

Linked Data

• MyVariant Identifiers: chr7:g.151845936T>A (hg19) ; chr7:g.152148851T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.152148851T>A , CM000669.2:g.152148851T>A	GRCh38
NC_000007.13:g.151845936T>A , CM000669.1:g.151845936T>A	GRCh37
NC_000007.12:g.151476869T>A	NCBI36
NG_033948.1:g.292155A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682040.1:c.1264A>T
ENST00000682116.1:n.2208A>T
ENST00000682283.1:c.13247A>T	ENSP00000507485.1:p.Lys4416Met
ENST00000682629.1:n.2376A>T
ENST00000683120.1:n.8268A>T
ENST00000683178.1:c.3649A>T
ENST00000683200.1:c.10586A>T	ENSP00000508052.1:p.Lys3529Met
ENST00000683337.1:n.4706A>T
ENST00000683502.1:c.3721A>T
ENST00000683621.1:n.1842A>T
ENST00000683640.1:n.1792A>T
ENST00000684069.1:c.1493A>T	ENSP00000507650.1:p.Lys498Met
ENST00000684261.1:c.7973A>T	ENSP00000508097.1:p.Lys2658Met
ENST00000684649.1:c.3721A>T
ENST00000262189.11:c.13076A>T MANE Select	ENSP00000262189.6:p.Lys4359Met
ENST00000360104.8:c.8863A>T
ENST00000418061.2:c.3718A>T
ENST00000424877.6:c.3652A>T
ENST00000679393.1:n.7787A>T
ENST00000679560.1:c.7976A>T	ENSP00000505094.1:p.Lys2659Met
ENST00000679882.1:c.12641A>T	ENSP00000506154.1:p.Lys4214Met
ENST00000680029.1:c.3653A>T
ENST00000680877.1:c.7976A>T	ENSP00000505724.1:p.Lys2659Met
ENST00000681923.1:n.2091A>T
ENST00000262189.10:c.13076A>T	ENSP00000262189.6:p.Lys4359Met
ENST00000355193.6:c.13076A>T	ENSP00000347325.3:p.Lys4359Met
ENST00000360104.7:c.5757A>T
ENST00000424877.5:c.2927A>T	ENSP00000410411.1:p.Lys976Met
ENST00000473186.5:n.10958A>T
ENST00000558084.5:c.*10596A>T	ENSP00000453752.1:n.*10596A>T
NM_170606.2:c.13076A>T	NP_733751.2:p.Lys4359Met
XM_005250025.3:c.13292A>T	XP_005250082.1:p.Lys4431Met
XM_005250026.2:c.13289A>T	XP_005250083.1:p.Lys4430Met
XM_005250027.3:c.13289A>T	XP_005250084.1:p.Lys4430Met
XM_005250028.3:c.13292A>T	XP_005250085.1:p.Lys4431Met
XM_005250031.3:c.13127A>T	XP_005250088.1:p.Lys4376Met
XM_006716077.2:c.13289A>T	XP_006716140.1:p.Lys4430Met
XM_006716078.2:c.13220A>T	XP_006716141.1:p.Lys4407Met
XM_006716079.2:c.13124A>T	XP_006716142.1:p.Lys4375Met
XM_011516450.1:c.13244A>T	XP_011514752.1:p.Lys4415Met
XM_011516451.1:c.13172A>T	XP_011514753.1:p.Lys4391Met
XM_011516452.1:c.13139A>T	XP_011514754.1:p.Lys4380Met
XM_011516453.1:c.13055A>T	XP_011514755.1:p.Lys4352Met
XM_011516454.1:c.12377A>T	XP_011514756.1:p.Lys4126Met
XM_011516455.1:c.10838A>T	XP_011514757.1:p.Lys3613Met
XM_011516456.1:c.13244A>T	XP_011514758.1:p.Lys4415Met
XM_005250025.4:c.13292A>T	XP_005250082.1:p.Lys4431Met
XM_005250026.3:c.13289A>T	XP_005250083.1:p.Lys4430Met
XM_005250027.4:c.13289A>T	XP_005250084.1:p.Lys4430Met
XM_005250028.4:c.13292A>T	XP_005250085.1:p.Lys4431Met
XM_005250031.4:c.13127A>T	XP_005250088.1:p.Lys4376Met
XM_006716077.3:c.13289A>T	XP_006716140.1:p.Lys4430Met
XM_006716078.3:c.13220A>T	XP_006716141.1:p.Lys4407Met
XM_006716079.3:c.13124A>T	XP_006716142.1:p.Lys4375Met
XM_011516450.2:c.13244A>T	XP_011514752.1:p.Lys4415Met
XM_011516451.2:c.13172A>T	XP_011514753.1:p.Lys4391Met
XM_011516452.2:c.13139A>T	XP_011514754.1:p.Lys4380Met
XM_011516453.2:c.13055A>T	XP_011514755.1:p.Lys4352Met
XM_011516454.2:c.12377A>T	XP_011514756.1:p.Lys4126Met
XM_011516456.2:c.13244A>T	XP_011514758.1:p.Lys4415Met
XM_017012480.1:c.13292A>T	XP_016867969.1:p.Lys4431Met
XM_017012481.1:c.13289A>T	XP_016867970.1:p.Lys4430Met
XM_017012482.1:c.13289A>T	XP_016867971.1:p.Lys4430Met
XM_017012483.1:c.13289A>T	XP_016867972.1:p.Lys4430Met
XM_017012484.1:c.13259A>T	XP_016867973.1:p.Lys4420Met
XM_017012485.1:c.13241A>T	XP_016867974.1:p.Lys4414Met
XM_017012486.1:c.13217A>T	XP_016867975.1:p.Lys4406Met
XM_017012487.1:c.13145A>T	XP_016867976.1:p.Lys4382Met
XM_017012488.1:c.13109A>T	XP_016867977.1:p.Lys4370Met
XM_017012489.1:c.9962A>T	XP_016867978.1:p.Lys3321Met
XM_017012490.2:c.9566A>T	XP_016867979.1:p.Lys3189Met
XM_024446852.1:c.13289A>T	XP_024302620.1:p.Lys4430Met
XM_024446853.1:c.13217A>T	XP_024302621.1:p.Lys4406Met
NM_170606.3:c.13076A>T MANE Select	NP_733751.2:p.Lys4359Met