Canonical Allele Identifier: CA458884757

Gene: KMT2C

Linked Data

• MyVariant Identifiers: chr7:g.151845893T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.152148808T>A , CM000669.2:g.152148808T>A	GRCh38
NC_000007.13:g.151845893T>A , CM000669.1:g.151845893T>A	GRCh37
NC_000007.12:g.151476826T>A	NCBI36
NG_033948.1:g.292198A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682040.1:c.1307A>T
ENST00000682116.1:n.2251A>T
ENST00000682283.1:c.13290A>T	ENSP00000507485.1:p.Pro4430=
ENST00000682629.1:n.2419A>T
ENST00000683120.1:n.8311A>T
ENST00000683178.1:c.3692A>T
ENST00000683200.1:c.10629A>T	ENSP00000508052.1:p.Pro3543=
ENST00000683337.1:n.4749A>T
ENST00000683502.1:c.3764A>T
ENST00000683621.1:n.1885A>T
ENST00000683640.1:n.1835A>T
ENST00000684069.1:c.1536A>T	ENSP00000507650.1:p.Pro512=
ENST00000684261.1:c.8016A>T	ENSP00000508097.1:p.Pro2672=
ENST00000684649.1:c.3764A>T
ENST00000262189.11:c.13119A>T MANE Select	ENSP00000262189.6:p.Pro4373=
ENST00000360104.8:c.8906A>T
ENST00000418061.2:c.3761A>T
ENST00000424877.6:c.3695A>T
ENST00000679393.1:n.7830A>T
ENST00000679560.1:c.8019A>T	ENSP00000505094.1:p.Pro2673=
ENST00000679882.1:c.12684A>T	ENSP00000506154.1:p.Pro4228=
ENST00000680029.1:c.3696A>T
ENST00000680877.1:c.8019A>T	ENSP00000505724.1:p.Pro2673=
ENST00000681923.1:n.2134A>T
ENST00000262189.10:c.13119A>T	ENSP00000262189.6:p.Pro4373=
ENST00000355193.6:c.13119A>T	ENSP00000347325.3:p.Pro4373=
ENST00000360104.7:c.5800A>T
ENST00000424877.5:c.2970A>T	ENSP00000410411.1:p.Pro990=
ENST00000473186.5:n.11001A>T
ENST00000558084.5:c.*10639A>T	ENSP00000453752.1:n.*10639A>T
NM_170606.2:c.13119A>T	NP_733751.2:p.Pro4373=
XM_005250025.3:c.13335A>T	XP_005250082.1:p.Pro4445=
XM_005250026.2:c.13332A>T	XP_005250083.1:p.Pro4444=
XM_005250027.3:c.13332A>T	XP_005250084.1:p.Pro4444=
XM_005250028.3:c.13335A>T	XP_005250085.1:p.Pro4445=
XM_005250031.3:c.13170A>T	XP_005250088.1:p.Pro4390=
XM_006716077.2:c.13332A>T	XP_006716140.1:p.Pro4444=
XM_006716078.2:c.13263A>T	XP_006716141.1:p.Pro4421=
XM_006716079.2:c.13167A>T	XP_006716142.1:p.Pro4389=
XM_011516450.1:c.13287A>T	XP_011514752.1:p.Pro4429=
XM_011516451.1:c.13215A>T	XP_011514753.1:p.Pro4405=
XM_011516452.1:c.13182A>T	XP_011514754.1:p.Pro4394=
XM_011516453.1:c.13098A>T	XP_011514755.1:p.Pro4366=
XM_011516454.1:c.12420A>T	XP_011514756.1:p.Pro4140=
XM_011516455.1:c.10881A>T	XP_011514757.1:p.Pro3627=
XM_011516456.1:c.13287A>T	XP_011514758.1:p.Pro4429=
XM_005250025.4:c.13335A>T	XP_005250082.1:p.Pro4445=
XM_005250026.3:c.13332A>T	XP_005250083.1:p.Pro4444=
XM_005250027.4:c.13332A>T	XP_005250084.1:p.Pro4444=
XM_005250028.4:c.13335A>T	XP_005250085.1:p.Pro4445=
XM_005250031.4:c.13170A>T	XP_005250088.1:p.Pro4390=
XM_006716077.3:c.13332A>T	XP_006716140.1:p.Pro4444=
XM_006716078.3:c.13263A>T	XP_006716141.1:p.Pro4421=
XM_006716079.3:c.13167A>T	XP_006716142.1:p.Pro4389=
XM_011516450.2:c.13287A>T	XP_011514752.1:p.Pro4429=
XM_011516451.2:c.13215A>T	XP_011514753.1:p.Pro4405=
XM_011516452.2:c.13182A>T	XP_011514754.1:p.Pro4394=
XM_011516453.2:c.13098A>T	XP_011514755.1:p.Pro4366=
XM_011516454.2:c.12420A>T	XP_011514756.1:p.Pro4140=
XM_011516456.2:c.13287A>T	XP_011514758.1:p.Pro4429=
XM_017012480.1:c.13335A>T	XP_016867969.1:p.Pro4445=
XM_017012481.1:c.13332A>T	XP_016867970.1:p.Pro4444=
XM_017012482.1:c.13332A>T	XP_016867971.1:p.Pro4444=
XM_017012483.1:c.13332A>T	XP_016867972.1:p.Pro4444=
XM_017012484.1:c.13302A>T	XP_016867973.1:p.Pro4434=
XM_017012485.1:c.13284A>T	XP_016867974.1:p.Pro4428=
XM_017012486.1:c.13260A>T	XP_016867975.1:p.Pro4420=
XM_017012487.1:c.13188A>T	XP_016867976.1:p.Pro4396=
XM_017012488.1:c.13152A>T	XP_016867977.1:p.Pro4384=
XM_017012489.1:c.10005A>T	XP_016867978.1:p.Pro3335=
XM_017012490.2:c.9609A>T	XP_016867979.1:p.Pro3203=
XM_024446852.1:c.13332A>T	XP_024302620.1:p.Pro4444=
XM_024446853.1:c.13260A>T	XP_024302621.1:p.Pro4420=
NM_170606.3:c.13119A>T MANE Select	NP_733751.2:p.Pro4373=