Canonical Allele Identifier: CA458884829

Gene: KMT2C

Linked Data

• MyVariant Identifiers: chr7:g.151845917T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.152148832T>A , CM000669.2:g.152148832T>A	GRCh38
NC_000007.13:g.151845917T>A , CM000669.1:g.151845917T>A	GRCh37
NC_000007.12:g.151476850T>A	NCBI36
NG_033948.1:g.292174A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682040.1:c.1283A>T
ENST00000682116.1:n.2227A>T
ENST00000682283.1:c.13266A>T	ENSP00000507485.1:p.Val4422=
ENST00000682629.1:n.2395A>T
ENST00000683120.1:n.8287A>T
ENST00000683178.1:c.3668A>T
ENST00000683200.1:c.10605A>T	ENSP00000508052.1:p.Val3535=
ENST00000683337.1:n.4725A>T
ENST00000683502.1:c.3740A>T
ENST00000683621.1:n.1861A>T
ENST00000683640.1:n.1811A>T
ENST00000684069.1:c.1512A>T	ENSP00000507650.1:p.Val504=
ENST00000684261.1:c.7992A>T	ENSP00000508097.1:p.Val2664=
ENST00000684649.1:c.3740A>T
ENST00000262189.11:c.13095A>T MANE Select	ENSP00000262189.6:p.Val4365=
ENST00000360104.8:c.8882A>T
ENST00000418061.2:c.3737A>T
ENST00000424877.6:c.3671A>T
ENST00000679393.1:n.7806A>T
ENST00000679560.1:c.7995A>T	ENSP00000505094.1:p.Val2665=
ENST00000679882.1:c.12660A>T	ENSP00000506154.1:p.Val4220=
ENST00000680029.1:c.3672A>T
ENST00000680877.1:c.7995A>T	ENSP00000505724.1:p.Val2665=
ENST00000681923.1:n.2110A>T
ENST00000262189.10:c.13095A>T	ENSP00000262189.6:p.Val4365=
ENST00000355193.6:c.13095A>T	ENSP00000347325.3:p.Val4365=
ENST00000360104.7:c.5776A>T
ENST00000424877.5:c.2946A>T	ENSP00000410411.1:p.Val982=
ENST00000473186.5:n.10977A>T
ENST00000558084.5:c.*10615A>T	ENSP00000453752.1:n.*10615A>T
NM_170606.2:c.13095A>T	NP_733751.2:p.Val4365=
XM_005250025.3:c.13311A>T	XP_005250082.1:p.Val4437=
XM_005250026.2:c.13308A>T	XP_005250083.1:p.Val4436=
XM_005250027.3:c.13308A>T	XP_005250084.1:p.Val4436=
XM_005250028.3:c.13311A>T	XP_005250085.1:p.Val4437=
XM_005250031.3:c.13146A>T	XP_005250088.1:p.Val4382=
XM_006716077.2:c.13308A>T	XP_006716140.1:p.Val4436=
XM_006716078.2:c.13239A>T	XP_006716141.1:p.Val4413=
XM_006716079.2:c.13143A>T	XP_006716142.1:p.Val4381=
XM_011516450.1:c.13263A>T	XP_011514752.1:p.Val4421=
XM_011516451.1:c.13191A>T	XP_011514753.1:p.Val4397=
XM_011516452.1:c.13158A>T	XP_011514754.1:p.Val4386=
XM_011516453.1:c.13074A>T	XP_011514755.1:p.Val4358=
XM_011516454.1:c.12396A>T	XP_011514756.1:p.Val4132=
XM_011516455.1:c.10857A>T	XP_011514757.1:p.Val3619=
XM_011516456.1:c.13263A>T	XP_011514758.1:p.Val4421=
XM_005250025.4:c.13311A>T	XP_005250082.1:p.Val4437=
XM_005250026.3:c.13308A>T	XP_005250083.1:p.Val4436=
XM_005250027.4:c.13308A>T	XP_005250084.1:p.Val4436=
XM_005250028.4:c.13311A>T	XP_005250085.1:p.Val4437=
XM_005250031.4:c.13146A>T	XP_005250088.1:p.Val4382=
XM_006716077.3:c.13308A>T	XP_006716140.1:p.Val4436=
XM_006716078.3:c.13239A>T	XP_006716141.1:p.Val4413=
XM_006716079.3:c.13143A>T	XP_006716142.1:p.Val4381=
XM_011516450.2:c.13263A>T	XP_011514752.1:p.Val4421=
XM_011516451.2:c.13191A>T	XP_011514753.1:p.Val4397=
XM_011516452.2:c.13158A>T	XP_011514754.1:p.Val4386=
XM_011516453.2:c.13074A>T	XP_011514755.1:p.Val4358=
XM_011516454.2:c.12396A>T	XP_011514756.1:p.Val4132=
XM_011516456.2:c.13263A>T	XP_011514758.1:p.Val4421=
XM_017012480.1:c.13311A>T	XP_016867969.1:p.Val4437=
XM_017012481.1:c.13308A>T	XP_016867970.1:p.Val4436=
XM_017012482.1:c.13308A>T	XP_016867971.1:p.Val4436=
XM_017012483.1:c.13308A>T	XP_016867972.1:p.Val4436=
XM_017012484.1:c.13278A>T	XP_016867973.1:p.Val4426=
XM_017012485.1:c.13260A>T	XP_016867974.1:p.Val4420=
XM_017012486.1:c.13236A>T	XP_016867975.1:p.Val4412=
XM_017012487.1:c.13164A>T	XP_016867976.1:p.Val4388=
XM_017012488.1:c.13128A>T	XP_016867977.1:p.Val4376=
XM_017012489.1:c.9981A>T	XP_016867978.1:p.Val3327=
XM_017012490.2:c.9585A>T	XP_016867979.1:p.Val3195=
XM_024446852.1:c.13308A>T	XP_024302620.1:p.Val4436=
XM_024446853.1:c.13236A>T	XP_024302621.1:p.Val4412=
NM_170606.3:c.13095A>T MANE Select	NP_733751.2:p.Val4365=