Canonical Allele Identifier: CA370093108

Gene: KMT2C

Linked Data

• MyVariant Identifiers: chr7:g.151845888C>T (hg19) ; chr7:g.152148803C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.152148803C>T , CM000669.2:g.152148803C>T	GRCh38
NC_000007.13:g.151845888C>T , CM000669.1:g.151845888C>T	GRCh37
NC_000007.12:g.151476821C>T	NCBI36
NG_033948.1:g.292203G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682040.1:c.1312G>A
ENST00000682116.1:n.2256G>A
ENST00000682283.1:c.13295G>A	ENSP00000507485.1:p.Cys4432Tyr
ENST00000682629.1:n.2424G>A
ENST00000683120.1:n.8316G>A
ENST00000683178.1:c.3697G>A
ENST00000683200.1:c.10634G>A	ENSP00000508052.1:p.Cys3545Tyr
ENST00000683337.1:n.4754G>A
ENST00000683502.1:c.3769G>A
ENST00000683621.1:n.1890G>A
ENST00000683640.1:n.1840G>A
ENST00000684069.1:c.1541G>A	ENSP00000507650.1:p.Cys514Tyr
ENST00000684261.1:c.8021G>A	ENSP00000508097.1:p.Cys2674Tyr
ENST00000684649.1:c.3769G>A
ENST00000262189.11:c.13124G>A MANE Select	ENSP00000262189.6:p.Cys4375Tyr
ENST00000360104.8:c.8911G>A
ENST00000418061.2:c.3766G>A
ENST00000424877.6:c.3700G>A
ENST00000679393.1:n.7835G>A
ENST00000679560.1:c.8024G>A	ENSP00000505094.1:p.Cys2675Tyr
ENST00000679882.1:c.12689G>A	ENSP00000506154.1:p.Cys4230Tyr
ENST00000680029.1:c.3701G>A
ENST00000680877.1:c.8024G>A	ENSP00000505724.1:p.Cys2675Tyr
ENST00000681923.1:n.2139G>A
ENST00000262189.10:c.13124G>A	ENSP00000262189.6:p.Cys4375Tyr
ENST00000355193.6:c.13124G>A	ENSP00000347325.3:p.Cys4375Tyr
ENST00000360104.7:c.5805G>A
ENST00000424877.5:c.2975G>A	ENSP00000410411.1:p.Cys992Tyr
ENST00000473186.5:n.11006G>A
ENST00000558084.5:c.*10644G>A	ENSP00000453752.1:n.*10644G>A
NM_170606.2:c.13124G>A	NP_733751.2:p.Cys4375Tyr
XM_005250025.3:c.13340G>A	XP_005250082.1:p.Cys4447Tyr
XM_005250026.2:c.13337G>A	XP_005250083.1:p.Cys4446Tyr
XM_005250027.3:c.13337G>A	XP_005250084.1:p.Cys4446Tyr
XM_005250028.3:c.13340G>A	XP_005250085.1:p.Cys4447Tyr
XM_005250031.3:c.13175G>A	XP_005250088.1:p.Cys4392Tyr
XM_006716077.2:c.13337G>A	XP_006716140.1:p.Cys4446Tyr
XM_006716078.2:c.13268G>A	XP_006716141.1:p.Cys4423Tyr
XM_006716079.2:c.13172G>A	XP_006716142.1:p.Cys4391Tyr
XM_011516450.1:c.13292G>A	XP_011514752.1:p.Cys4431Tyr
XM_011516451.1:c.13220G>A	XP_011514753.1:p.Cys4407Tyr
XM_011516452.1:c.13187G>A	XP_011514754.1:p.Cys4396Tyr
XM_011516453.1:c.13103G>A	XP_011514755.1:p.Cys4368Tyr
XM_011516454.1:c.12425G>A	XP_011514756.1:p.Cys4142Tyr
XM_011516455.1:c.10886G>A	XP_011514757.1:p.Cys3629Tyr
XM_011516456.1:c.13292G>A	XP_011514758.1:p.Cys4431Tyr
XM_005250025.4:c.13340G>A	XP_005250082.1:p.Cys4447Tyr
XM_005250026.3:c.13337G>A	XP_005250083.1:p.Cys4446Tyr
XM_005250027.4:c.13337G>A	XP_005250084.1:p.Cys4446Tyr
XM_005250028.4:c.13340G>A	XP_005250085.1:p.Cys4447Tyr
XM_005250031.4:c.13175G>A	XP_005250088.1:p.Cys4392Tyr
XM_006716077.3:c.13337G>A	XP_006716140.1:p.Cys4446Tyr
XM_006716078.3:c.13268G>A	XP_006716141.1:p.Cys4423Tyr
XM_006716079.3:c.13172G>A	XP_006716142.1:p.Cys4391Tyr
XM_011516450.2:c.13292G>A	XP_011514752.1:p.Cys4431Tyr
XM_011516451.2:c.13220G>A	XP_011514753.1:p.Cys4407Tyr
XM_011516452.2:c.13187G>A	XP_011514754.1:p.Cys4396Tyr
XM_011516453.2:c.13103G>A	XP_011514755.1:p.Cys4368Tyr
XM_011516454.2:c.12425G>A	XP_011514756.1:p.Cys4142Tyr
XM_011516456.2:c.13292G>A	XP_011514758.1:p.Cys4431Tyr
XM_017012480.1:c.13340G>A	XP_016867969.1:p.Cys4447Tyr
XM_017012481.1:c.13337G>A	XP_016867970.1:p.Cys4446Tyr
XM_017012482.1:c.13337G>A	XP_016867971.1:p.Cys4446Tyr
XM_017012483.1:c.13337G>A	XP_016867972.1:p.Cys4446Tyr
XM_017012484.1:c.13307G>A	XP_016867973.1:p.Cys4436Tyr
XM_017012485.1:c.13289G>A	XP_016867974.1:p.Cys4430Tyr
XM_017012486.1:c.13265G>A	XP_016867975.1:p.Cys4422Tyr
XM_017012487.1:c.13193G>A	XP_016867976.1:p.Cys4398Tyr
XM_017012488.1:c.13157G>A	XP_016867977.1:p.Cys4386Tyr
XM_017012489.1:c.10010G>A	XP_016867978.1:p.Cys3337Tyr
XM_017012490.2:c.9614G>A	XP_016867979.1:p.Cys3205Tyr
XM_024446852.1:c.13337G>A	XP_024302620.1:p.Cys4446Tyr
XM_024446853.1:c.13265G>A	XP_024302621.1:p.Cys4422Tyr
NM_170606.3:c.13124G>A MANE Select	NP_733751.2:p.Cys4375Tyr