Canonical Allele Identifier: CA370093010

Gene: KMT2C

Linked Data

• MyVariant Identifiers: chr7:g.151845862T>A (hg19) ; chr7:g.152148777T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.152148777T>A , CM000669.2:g.152148777T>A	GRCh38
NC_000007.13:g.151845862T>A , CM000669.1:g.151845862T>A	GRCh37
NC_000007.12:g.151476795T>A	NCBI36
NG_033948.1:g.292229A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000682040.1:c.1338A>T
ENST00000682116.1:n.2282A>T
ENST00000682283.1:c.13321A>T	ENSP00000507485.1:p.Lys4441Ter
ENST00000682629.1:n.2450A>T
ENST00000683120.1:n.8342A>T
ENST00000683178.1:c.3723A>T
ENST00000683200.1:c.10660A>T	ENSP00000508052.1:p.Lys3554Ter
ENST00000683337.1:n.4780A>T
ENST00000683502.1:c.3795A>T
ENST00000683621.1:n.1916A>T
ENST00000683640.1:n.1866A>T
ENST00000684069.1:c.1567A>T	ENSP00000507650.1:p.Lys523Ter
ENST00000684261.1:c.8047A>T	ENSP00000508097.1:p.Lys2683Ter
ENST00000684649.1:c.3795A>T
ENST00000262189.11:c.13150A>T MANE Select	ENSP00000262189.6:p.Lys4384Ter
ENST00000360104.8:c.8937A>T
ENST00000418061.2:c.3792A>T
ENST00000424877.6:c.3726A>T
ENST00000679393.1:n.7861A>T
ENST00000679560.1:c.8050A>T	ENSP00000505094.1:p.Lys2684Ter
ENST00000679882.1:c.12715A>T	ENSP00000506154.1:p.Lys4239Ter
ENST00000680029.1:c.3727A>T
ENST00000680877.1:c.8050A>T	ENSP00000505724.1:p.Lys2684Ter
ENST00000681923.1:n.2165A>T
ENST00000262189.10:c.13150A>T	ENSP00000262189.6:p.Lys4384Ter
ENST00000355193.6:c.13150A>T	ENSP00000347325.3:p.Lys4384Ter
ENST00000360104.7:c.5831A>T
ENST00000424877.5:c.3001A>T	ENSP00000410411.1:p.Lys1001Ter
ENST00000473186.5:n.11032A>T
ENST00000558084.5:c.*10670A>T	ENSP00000453752.1:n.*10670A>T
NM_170606.2:c.13150A>T	NP_733751.2:p.Lys4384Ter
XM_005250025.3:c.13366A>T	XP_005250082.1:p.Lys4456Ter
XM_005250026.2:c.13363A>T	XP_005250083.1:p.Lys4455Ter
XM_005250027.3:c.13363A>T	XP_005250084.1:p.Lys4455Ter
XM_005250028.3:c.13366A>T	XP_005250085.1:p.Lys4456Ter
XM_005250031.3:c.13201A>T	XP_005250088.1:p.Lys4401Ter
XM_006716077.2:c.13363A>T	XP_006716140.1:p.Lys4455Ter
XM_006716078.2:c.13294A>T	XP_006716141.1:p.Lys4432Ter
XM_006716079.2:c.13198A>T	XP_006716142.1:p.Lys4400Ter
XM_011516450.1:c.13318A>T	XP_011514752.1:p.Lys4440Ter
XM_011516451.1:c.13246A>T	XP_011514753.1:p.Lys4416Ter
XM_011516452.1:c.13213A>T	XP_011514754.1:p.Lys4405Ter
XM_011516453.1:c.13129A>T	XP_011514755.1:p.Lys4377Ter
XM_011516454.1:c.12451A>T	XP_011514756.1:p.Lys4151Ter
XM_011516455.1:c.10912A>T	XP_011514757.1:p.Lys3638Ter
XM_011516456.1:c.13318A>T	XP_011514758.1:p.Lys4440Ter
XM_005250025.4:c.13366A>T	XP_005250082.1:p.Lys4456Ter
XM_005250026.3:c.13363A>T	XP_005250083.1:p.Lys4455Ter
XM_005250027.4:c.13363A>T	XP_005250084.1:p.Lys4455Ter
XM_005250028.4:c.13366A>T	XP_005250085.1:p.Lys4456Ter
XM_005250031.4:c.13201A>T	XP_005250088.1:p.Lys4401Ter
XM_006716077.3:c.13363A>T	XP_006716140.1:p.Lys4455Ter
XM_006716078.3:c.13294A>T	XP_006716141.1:p.Lys4432Ter
XM_006716079.3:c.13198A>T	XP_006716142.1:p.Lys4400Ter
XM_011516450.2:c.13318A>T	XP_011514752.1:p.Lys4440Ter
XM_011516451.2:c.13246A>T	XP_011514753.1:p.Lys4416Ter
XM_011516452.2:c.13213A>T	XP_011514754.1:p.Lys4405Ter
XM_011516453.2:c.13129A>T	XP_011514755.1:p.Lys4377Ter
XM_011516454.2:c.12451A>T	XP_011514756.1:p.Lys4151Ter
XM_011516456.2:c.13318A>T	XP_011514758.1:p.Lys4440Ter
XM_017012480.1:c.13366A>T	XP_016867969.1:p.Lys4456Ter
XM_017012481.1:c.13363A>T	XP_016867970.1:p.Lys4455Ter
XM_017012482.1:c.13363A>T	XP_016867971.1:p.Lys4455Ter
XM_017012483.1:c.13363A>T	XP_016867972.1:p.Lys4455Ter
XM_017012484.1:c.13333A>T	XP_016867973.1:p.Lys4445Ter
XM_017012485.1:c.13315A>T	XP_016867974.1:p.Lys4439Ter
XM_017012486.1:c.13291A>T	XP_016867975.1:p.Lys4431Ter
XM_017012487.1:c.13219A>T	XP_016867976.1:p.Lys4407Ter
XM_017012488.1:c.13183A>T	XP_016867977.1:p.Lys4395Ter
XM_017012489.1:c.10036A>T	XP_016867978.1:p.Lys3346Ter
XM_017012490.2:c.9640A>T	XP_016867979.1:p.Lys3214Ter
XM_024446852.1:c.13363A>T	XP_024302620.1:p.Lys4455Ter
XM_024446853.1:c.13291A>T	XP_024302621.1:p.Lys4431Ter
NM_170606.3:c.13150A>T MANE Select	NP_733751.2:p.Lys4384Ter