Canonical Allele Identifier: CA458884957

Gene: KMT2C

Linked Data

• MyVariant Identifiers: chr7:g.151845764T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.152148679T>G , CM000669.2:g.152148679T>G	GRCh38
NC_000007.13:g.151845764T>G , CM000669.1:g.151845764T>G	GRCh37
NC_000007.12:g.151476697T>G	NCBI36
NG_033948.1:g.292327A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000682040.1:c.1436A>C
ENST00000682116.1:n.2380A>C
ENST00000682283.1:c.13419A>C	ENSP00000507485.1:p.Pro4473=
ENST00000682629.1:n.2548A>C
ENST00000683120.1:n.8440A>C
ENST00000683178.1:c.3821A>C
ENST00000683200.1:c.10758A>C	ENSP00000508052.1:p.Pro3586=
ENST00000683337.1:n.4878A>C
ENST00000683502.1:c.3893A>C
ENST00000683621.1:n.2014A>C
ENST00000683640.1:n.1964A>C
ENST00000684069.1:c.1665A>C	ENSP00000507650.1:p.Pro555=
ENST00000684261.1:c.8145A>C	ENSP00000508097.1:p.Pro2715=
ENST00000684391.1:n.6A>C
ENST00000684649.1:c.3893A>C
ENST00000262189.11:c.13248A>C MANE Select	ENSP00000262189.6:p.Pro4416=
ENST00000360104.8:c.9035A>C
ENST00000418061.2:c.3890A>C
ENST00000424877.6:c.3824A>C
ENST00000679393.1:n.7959A>C
ENST00000679560.1:c.8148A>C	ENSP00000505094.1:p.Pro2716=
ENST00000679882.1:c.12813A>C	ENSP00000506154.1:p.Pro4271=
ENST00000680029.1:c.3825A>C
ENST00000680877.1:c.8148A>C	ENSP00000505724.1:p.Pro2716=
ENST00000681923.1:n.2263A>C
ENST00000262189.10:c.13248A>C	ENSP00000262189.6:p.Pro4416=
ENST00000355193.6:c.13248A>C	ENSP00000347325.3:p.Pro4416=
ENST00000360104.7:c.5929A>C
ENST00000424877.5:c.3099A>C	ENSP00000410411.1:p.Pro1033=
ENST00000473186.5:n.11130A>C
ENST00000558084.5:c.*10768A>C	ENSP00000453752.1:n.*10768A>C
NM_170606.2:c.13248A>C	NP_733751.2:p.Pro4416=
XM_005250025.3:c.13464A>C	XP_005250082.1:p.Pro4488=
XM_005250026.2:c.13461A>C	XP_005250083.1:p.Pro4487=
XM_005250027.3:c.13461A>C	XP_005250084.1:p.Pro4487=
XM_005250028.3:c.13464A>C	XP_005250085.1:p.Pro4488=
XM_005250031.3:c.13299A>C	XP_005250088.1:p.Pro4433=
XM_006716077.2:c.13461A>C	XP_006716140.1:p.Pro4487=
XM_006716078.2:c.13392A>C	XP_006716141.1:p.Pro4464=
XM_006716079.2:c.13296A>C	XP_006716142.1:p.Pro4432=
XM_011516450.1:c.13416A>C	XP_011514752.1:p.Pro4472=
XM_011516451.1:c.13344A>C	XP_011514753.1:p.Pro4448=
XM_011516452.1:c.13311A>C	XP_011514754.1:p.Pro4437=
XM_011516453.1:c.13227A>C	XP_011514755.1:p.Pro4409=
XM_011516454.1:c.12549A>C	XP_011514756.1:p.Pro4183=
XM_011516455.1:c.11010A>C	XP_011514757.1:p.Pro3670=
XM_011516456.1:c.13416A>C	XP_011514758.1:p.Pro4472=
XM_005250025.4:c.13464A>C	XP_005250082.1:p.Pro4488=
XM_005250026.3:c.13461A>C	XP_005250083.1:p.Pro4487=
XM_005250027.4:c.13461A>C	XP_005250084.1:p.Pro4487=
XM_005250028.4:c.13464A>C	XP_005250085.1:p.Pro4488=
XM_005250031.4:c.13299A>C	XP_005250088.1:p.Pro4433=
XM_006716077.3:c.13461A>C	XP_006716140.1:p.Pro4487=
XM_006716078.3:c.13392A>C	XP_006716141.1:p.Pro4464=
XM_006716079.3:c.13296A>C	XP_006716142.1:p.Pro4432=
XM_011516450.2:c.13416A>C	XP_011514752.1:p.Pro4472=
XM_011516451.2:c.13344A>C	XP_011514753.1:p.Pro4448=
XM_011516452.2:c.13311A>C	XP_011514754.1:p.Pro4437=
XM_011516453.2:c.13227A>C	XP_011514755.1:p.Pro4409=
XM_011516454.2:c.12549A>C	XP_011514756.1:p.Pro4183=
XM_011516456.2:c.13416A>C	XP_011514758.1:p.Pro4472=
XM_017012480.1:c.13464A>C	XP_016867969.1:p.Pro4488=
XM_017012481.1:c.13461A>C	XP_016867970.1:p.Pro4487=
XM_017012482.1:c.13461A>C	XP_016867971.1:p.Pro4487=
XM_017012483.1:c.13461A>C	XP_016867972.1:p.Pro4487=
XM_017012484.1:c.13431A>C	XP_016867973.1:p.Pro4477=
XM_017012485.1:c.13413A>C	XP_016867974.1:p.Pro4471=
XM_017012486.1:c.13389A>C	XP_016867975.1:p.Pro4463=
XM_017012487.1:c.13317A>C	XP_016867976.1:p.Pro4439=
XM_017012488.1:c.13281A>C	XP_016867977.1:p.Pro4427=
XM_017012489.1:c.10134A>C	XP_016867978.1:p.Pro3378=
XM_017012490.2:c.9738A>C	XP_016867979.1:p.Pro3246=
XM_024446852.1:c.13461A>C	XP_024302620.1:p.Pro4487=
XM_024446853.1:c.13389A>C	XP_024302621.1:p.Pro4463=
NM_170606.3:c.13248A>C MANE Select	NP_733751.2:p.Pro4416=