Canonical Allele Identifier: CA370093314

Gene: KMT2C

Linked Data

• MyVariant Identifiers: chr7:g.151845948A>T (hg19) ; chr7:g.152148863A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.152148863A>T , CM000669.2:g.152148863A>T	GRCh38
NC_000007.13:g.151845948A>T , CM000669.1:g.151845948A>T	GRCh37
NC_000007.12:g.151476881A>T	NCBI36
NG_033948.1:g.292143T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682040.1:c.1252T>A
ENST00000682116.1:n.2196T>A
ENST00000682283.1:c.13235T>A	ENSP00000507485.1:p.Met4412Lys
ENST00000682629.1:n.2364T>A
ENST00000683120.1:n.8256T>A
ENST00000683178.1:c.3637T>A
ENST00000683200.1:c.10574T>A	ENSP00000508052.1:p.Met3525Lys
ENST00000683337.1:n.4694T>A
ENST00000683502.1:c.3709T>A
ENST00000683621.1:n.1830T>A
ENST00000683640.1:n.1780T>A
ENST00000684069.1:c.1481T>A	ENSP00000507650.1:p.Met494Lys
ENST00000684261.1:c.7961T>A	ENSP00000508097.1:p.Met2654Lys
ENST00000684649.1:c.3709T>A
ENST00000262189.11:c.13064T>A MANE Select	ENSP00000262189.6:p.Met4355Lys
ENST00000360104.8:c.8851T>A
ENST00000418061.2:c.3706T>A
ENST00000424877.6:c.3640T>A
ENST00000679393.1:n.7775T>A
ENST00000679560.1:c.7964T>A	ENSP00000505094.1:p.Met2655Lys
ENST00000679882.1:c.12629T>A	ENSP00000506154.1:p.Met4210Lys
ENST00000680029.1:c.3641T>A
ENST00000680877.1:c.7964T>A	ENSP00000505724.1:p.Met2655Lys
ENST00000681923.1:n.2079T>A
ENST00000262189.10:c.13064T>A	ENSP00000262189.6:p.Met4355Lys
ENST00000355193.6:c.13064T>A	ENSP00000347325.3:p.Met4355Lys
ENST00000360104.7:c.5745T>A
ENST00000424877.5:c.2915T>A	ENSP00000410411.1:p.Met972Lys
ENST00000473186.5:n.10946T>A
ENST00000558084.5:c.*10584T>A	ENSP00000453752.1:n.*10584T>A
NM_170606.2:c.13064T>A	NP_733751.2:p.Met4355Lys
XM_005250025.3:c.13280T>A	XP_005250082.1:p.Met4427Lys
XM_005250026.2:c.13277T>A	XP_005250083.1:p.Met4426Lys
XM_005250027.3:c.13277T>A	XP_005250084.1:p.Met4426Lys
XM_005250028.3:c.13280T>A	XP_005250085.1:p.Met4427Lys
XM_005250031.3:c.13115T>A	XP_005250088.1:p.Met4372Lys
XM_006716077.2:c.13277T>A	XP_006716140.1:p.Met4426Lys
XM_006716078.2:c.13208T>A	XP_006716141.1:p.Met4403Lys
XM_006716079.2:c.13112T>A	XP_006716142.1:p.Met4371Lys
XM_011516450.1:c.13232T>A	XP_011514752.1:p.Met4411Lys
XM_011516451.1:c.13160T>A	XP_011514753.1:p.Met4387Lys
XM_011516452.1:c.13127T>A	XP_011514754.1:p.Met4376Lys
XM_011516453.1:c.13043T>A	XP_011514755.1:p.Met4348Lys
XM_011516454.1:c.12365T>A	XP_011514756.1:p.Met4122Lys
XM_011516455.1:c.10826T>A	XP_011514757.1:p.Met3609Lys
XM_011516456.1:c.13232T>A	XP_011514758.1:p.Met4411Lys
XM_005250025.4:c.13280T>A	XP_005250082.1:p.Met4427Lys
XM_005250026.3:c.13277T>A	XP_005250083.1:p.Met4426Lys
XM_005250027.4:c.13277T>A	XP_005250084.1:p.Met4426Lys
XM_005250028.4:c.13280T>A	XP_005250085.1:p.Met4427Lys
XM_005250031.4:c.13115T>A	XP_005250088.1:p.Met4372Lys
XM_006716077.3:c.13277T>A	XP_006716140.1:p.Met4426Lys
XM_006716078.3:c.13208T>A	XP_006716141.1:p.Met4403Lys
XM_006716079.3:c.13112T>A	XP_006716142.1:p.Met4371Lys
XM_011516450.2:c.13232T>A	XP_011514752.1:p.Met4411Lys
XM_011516451.2:c.13160T>A	XP_011514753.1:p.Met4387Lys
XM_011516452.2:c.13127T>A	XP_011514754.1:p.Met4376Lys
XM_011516453.2:c.13043T>A	XP_011514755.1:p.Met4348Lys
XM_011516454.2:c.12365T>A	XP_011514756.1:p.Met4122Lys
XM_011516456.2:c.13232T>A	XP_011514758.1:p.Met4411Lys
XM_017012480.1:c.13280T>A	XP_016867969.1:p.Met4427Lys
XM_017012481.1:c.13277T>A	XP_016867970.1:p.Met4426Lys
XM_017012482.1:c.13277T>A	XP_016867971.1:p.Met4426Lys
XM_017012483.1:c.13277T>A	XP_016867972.1:p.Met4426Lys
XM_017012484.1:c.13247T>A	XP_016867973.1:p.Met4416Lys
XM_017012485.1:c.13229T>A	XP_016867974.1:p.Met4410Lys
XM_017012486.1:c.13205T>A	XP_016867975.1:p.Met4402Lys
XM_017012487.1:c.13133T>A	XP_016867976.1:p.Met4378Lys
XM_017012488.1:c.13097T>A	XP_016867977.1:p.Met4366Lys
XM_017012489.1:c.9950T>A	XP_016867978.1:p.Met3317Lys
XM_017012490.2:c.9554T>A	XP_016867979.1:p.Met3185Lys
XM_024446852.1:c.13277T>A	XP_024302620.1:p.Met4426Lys
XM_024446853.1:c.13205T>A	XP_024302621.1:p.Met4402Lys
NM_170606.3:c.13064T>A MANE Select	NP_733751.2:p.Met4355Lys