Canonical Allele Identifier: CA370091861

Gene: KMT2C

Linked Data

• MyVariant Identifiers: chr7:g.151845771T>A (hg19) ; chr7:g.152148686T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.152148686T>A , CM000669.2:g.152148686T>A	GRCh38
NC_000007.13:g.151845771T>A , CM000669.1:g.151845771T>A	GRCh37
NC_000007.12:g.151476704T>A	NCBI36
NG_033948.1:g.292320A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000682040.1:c.1429A>T
ENST00000682116.1:n.2373A>T
ENST00000682283.1:c.13412A>T	ENSP00000507485.1:p.Asp4471Val
ENST00000682629.1:n.2541A>T
ENST00000683120.1:n.8433A>T
ENST00000683178.1:c.3814A>T
ENST00000683200.1:c.10751A>T	ENSP00000508052.1:p.Asp3584Val
ENST00000683337.1:n.4871A>T
ENST00000683502.1:c.3886A>T
ENST00000683621.1:n.2007A>T
ENST00000683640.1:n.1957A>T
ENST00000684069.1:c.1658A>T	ENSP00000507650.1:p.Asp553Val
ENST00000684261.1:c.8138A>T	ENSP00000508097.1:p.Asp2713Val
ENST00000684649.1:c.3886A>T
ENST00000262189.11:c.13241A>T MANE Select	ENSP00000262189.6:p.Asp4414Val
ENST00000360104.8:c.9028A>T
ENST00000418061.2:c.3883A>T
ENST00000424877.6:c.3817A>T
ENST00000679393.1:n.7952A>T
ENST00000679560.1:c.8141A>T	ENSP00000505094.1:p.Asp2714Val
ENST00000679882.1:c.12806A>T	ENSP00000506154.1:p.Asp4269Val
ENST00000680029.1:c.3818A>T
ENST00000680877.1:c.8141A>T	ENSP00000505724.1:p.Asp2714Val
ENST00000681923.1:n.2256A>T
ENST00000262189.10:c.13241A>T	ENSP00000262189.6:p.Asp4414Val
ENST00000355193.6:c.13241A>T	ENSP00000347325.3:p.Asp4414Val
ENST00000360104.7:c.5922A>T
ENST00000424877.5:c.3092A>T	ENSP00000410411.1:p.Asp1031Val
ENST00000473186.5:n.11123A>T
ENST00000558084.5:c.*10761A>T	ENSP00000453752.1:n.*10761A>T
NM_170606.2:c.13241A>T	NP_733751.2:p.Asp4414Val
XM_005250025.3:c.13457A>T	XP_005250082.1:p.Asp4486Val
XM_005250026.2:c.13454A>T	XP_005250083.1:p.Asp4485Val
XM_005250027.3:c.13454A>T	XP_005250084.1:p.Asp4485Val
XM_005250028.3:c.13457A>T	XP_005250085.1:p.Asp4486Val
XM_005250031.3:c.13292A>T	XP_005250088.1:p.Asp4431Val
XM_006716077.2:c.13454A>T	XP_006716140.1:p.Asp4485Val
XM_006716078.2:c.13385A>T	XP_006716141.1:p.Asp4462Val
XM_006716079.2:c.13289A>T	XP_006716142.1:p.Asp4430Val
XM_011516450.1:c.13409A>T	XP_011514752.1:p.Asp4470Val
XM_011516451.1:c.13337A>T	XP_011514753.1:p.Asp4446Val
XM_011516452.1:c.13304A>T	XP_011514754.1:p.Asp4435Val
XM_011516453.1:c.13220A>T	XP_011514755.1:p.Asp4407Val
XM_011516454.1:c.12542A>T	XP_011514756.1:p.Asp4181Val
XM_011516455.1:c.11003A>T	XP_011514757.1:p.Asp3668Val
XM_011516456.1:c.13409A>T	XP_011514758.1:p.Asp4470Val
XM_005250025.4:c.13457A>T	XP_005250082.1:p.Asp4486Val
XM_005250026.3:c.13454A>T	XP_005250083.1:p.Asp4485Val
XM_005250027.4:c.13454A>T	XP_005250084.1:p.Asp4485Val
XM_005250028.4:c.13457A>T	XP_005250085.1:p.Asp4486Val
XM_005250031.4:c.13292A>T	XP_005250088.1:p.Asp4431Val
XM_006716077.3:c.13454A>T	XP_006716140.1:p.Asp4485Val
XM_006716078.3:c.13385A>T	XP_006716141.1:p.Asp4462Val
XM_006716079.3:c.13289A>T	XP_006716142.1:p.Asp4430Val
XM_011516450.2:c.13409A>T	XP_011514752.1:p.Asp4470Val
XM_011516451.2:c.13337A>T	XP_011514753.1:p.Asp4446Val
XM_011516452.2:c.13304A>T	XP_011514754.1:p.Asp4435Val
XM_011516453.2:c.13220A>T	XP_011514755.1:p.Asp4407Val
XM_011516454.2:c.12542A>T	XP_011514756.1:p.Asp4181Val
XM_011516456.2:c.13409A>T	XP_011514758.1:p.Asp4470Val
XM_017012480.1:c.13457A>T	XP_016867969.1:p.Asp4486Val
XM_017012481.1:c.13454A>T	XP_016867970.1:p.Asp4485Val
XM_017012482.1:c.13454A>T	XP_016867971.1:p.Asp4485Val
XM_017012483.1:c.13454A>T	XP_016867972.1:p.Asp4485Val
XM_017012484.1:c.13424A>T	XP_016867973.1:p.Asp4475Val
XM_017012485.1:c.13406A>T	XP_016867974.1:p.Asp4469Val
XM_017012486.1:c.13382A>T	XP_016867975.1:p.Asp4461Val
XM_017012487.1:c.13310A>T	XP_016867976.1:p.Asp4437Val
XM_017012488.1:c.13274A>T	XP_016867977.1:p.Asp4425Val
XM_017012489.1:c.10127A>T	XP_016867978.1:p.Asp3376Val
XM_017012490.2:c.9731A>T	XP_016867979.1:p.Asp3244Val
XM_024446852.1:c.13454A>T	XP_024302620.1:p.Asp4485Val
XM_024446853.1:c.13382A>T	XP_024302621.1:p.Asp4461Val
NM_170606.3:c.13241A>T MANE Select	NP_733751.2:p.Asp4414Val