Canonical Allele Identifier: CA370093359

Gene: KMT2C

Linked Data

• MyVariant Identifiers: chr7:g.151845960T>G (hg19) ; chr7:g.152148875T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.152148875T>G , CM000669.2:g.152148875T>G	GRCh38
NC_000007.13:g.151845960T>G , CM000669.1:g.151845960T>G	GRCh37
NC_000007.12:g.151476893T>G	NCBI36
NG_033948.1:g.292131A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682040.1:c.1240A>C
ENST00000682116.1:n.2184A>C
ENST00000682283.1:c.13223A>C	ENSP00000507485.1:p.Lys4408Thr
ENST00000682629.1:n.2352A>C
ENST00000683120.1:n.8244A>C
ENST00000683178.1:c.3625A>C
ENST00000683200.1:c.10562A>C	ENSP00000508052.1:p.Lys3521Thr
ENST00000683337.1:n.4682A>C
ENST00000683502.1:c.3697A>C
ENST00000683621.1:n.1818A>C
ENST00000683640.1:n.1768A>C
ENST00000684069.1:c.1469A>C	ENSP00000507650.1:p.Lys490Thr
ENST00000684261.1:c.7949A>C	ENSP00000508097.1:p.Lys2650Thr
ENST00000684649.1:c.3697A>C
ENST00000262189.11:c.13052A>C MANE Select	ENSP00000262189.6:p.Lys4351Thr
ENST00000360104.8:c.8839A>C
ENST00000418061.2:c.3694A>C
ENST00000424877.6:c.3628A>C
ENST00000679393.1:n.7763A>C
ENST00000679560.1:c.7952A>C	ENSP00000505094.1:p.Lys2651Thr
ENST00000679882.1:c.12617A>C	ENSP00000506154.1:p.Lys4206Thr
ENST00000680029.1:c.3629A>C
ENST00000680877.1:c.7952A>C	ENSP00000505724.1:p.Lys2651Thr
ENST00000681923.1:n.2067A>C
ENST00000262189.10:c.13052A>C	ENSP00000262189.6:p.Lys4351Thr
ENST00000355193.6:c.13052A>C	ENSP00000347325.3:p.Lys4351Thr
ENST00000360104.7:c.5733A>C
ENST00000424877.5:c.2903A>C	ENSP00000410411.1:p.Lys968Thr
ENST00000473186.5:n.10934A>C
ENST00000558084.5:c.*10572A>C	ENSP00000453752.1:n.*10572A>C
NM_170606.2:c.13052A>C	NP_733751.2:p.Lys4351Thr
XM_005250025.3:c.13268A>C	XP_005250082.1:p.Lys4423Thr
XM_005250026.2:c.13265A>C	XP_005250083.1:p.Lys4422Thr
XM_005250027.3:c.13265A>C	XP_005250084.1:p.Lys4422Thr
XM_005250028.3:c.13268A>C	XP_005250085.1:p.Lys4423Thr
XM_005250031.3:c.13103A>C	XP_005250088.1:p.Lys4368Thr
XM_006716077.2:c.13265A>C	XP_006716140.1:p.Lys4422Thr
XM_006716078.2:c.13196A>C	XP_006716141.1:p.Lys4399Thr
XM_006716079.2:c.13100A>C	XP_006716142.1:p.Lys4367Thr
XM_011516450.1:c.13220A>C	XP_011514752.1:p.Lys4407Thr
XM_011516451.1:c.13148A>C	XP_011514753.1:p.Lys4383Thr
XM_011516452.1:c.13115A>C	XP_011514754.1:p.Lys4372Thr
XM_011516453.1:c.13031A>C	XP_011514755.1:p.Lys4344Thr
XM_011516454.1:c.12353A>C	XP_011514756.1:p.Lys4118Thr
XM_011516455.1:c.10814A>C	XP_011514757.1:p.Lys3605Thr
XM_011516456.1:c.13220A>C	XP_011514758.1:p.Lys4407Thr
XM_005250025.4:c.13268A>C	XP_005250082.1:p.Lys4423Thr
XM_005250026.3:c.13265A>C	XP_005250083.1:p.Lys4422Thr
XM_005250027.4:c.13265A>C	XP_005250084.1:p.Lys4422Thr
XM_005250028.4:c.13268A>C	XP_005250085.1:p.Lys4423Thr
XM_005250031.4:c.13103A>C	XP_005250088.1:p.Lys4368Thr
XM_006716077.3:c.13265A>C	XP_006716140.1:p.Lys4422Thr
XM_006716078.3:c.13196A>C	XP_006716141.1:p.Lys4399Thr
XM_006716079.3:c.13100A>C	XP_006716142.1:p.Lys4367Thr
XM_011516450.2:c.13220A>C	XP_011514752.1:p.Lys4407Thr
XM_011516451.2:c.13148A>C	XP_011514753.1:p.Lys4383Thr
XM_011516452.2:c.13115A>C	XP_011514754.1:p.Lys4372Thr
XM_011516453.2:c.13031A>C	XP_011514755.1:p.Lys4344Thr
XM_011516454.2:c.12353A>C	XP_011514756.1:p.Lys4118Thr
XM_011516456.2:c.13220A>C	XP_011514758.1:p.Lys4407Thr
XM_017012480.1:c.13268A>C	XP_016867969.1:p.Lys4423Thr
XM_017012481.1:c.13265A>C	XP_016867970.1:p.Lys4422Thr
XM_017012482.1:c.13265A>C	XP_016867971.1:p.Lys4422Thr
XM_017012483.1:c.13265A>C	XP_016867972.1:p.Lys4422Thr
XM_017012484.1:c.13235A>C	XP_016867973.1:p.Lys4412Thr
XM_017012485.1:c.13217A>C	XP_016867974.1:p.Lys4406Thr
XM_017012486.1:c.13193A>C	XP_016867975.1:p.Lys4398Thr
XM_017012487.1:c.13121A>C	XP_016867976.1:p.Lys4374Thr
XM_017012488.1:c.13085A>C	XP_016867977.1:p.Lys4362Thr
XM_017012489.1:c.9938A>C	XP_016867978.1:p.Lys3313Thr
XM_017012490.2:c.9542A>C	XP_016867979.1:p.Lys3181Thr
XM_024446852.1:c.13265A>C	XP_024302620.1:p.Lys4422Thr
XM_024446853.1:c.13193A>C	XP_024302621.1:p.Lys4398Thr
NM_170606.3:c.13052A>C MANE Select	NP_733751.2:p.Lys4351Thr