Canonical Allele Identifier: CA370092828

Gene: KMT2C

Linked Data

• MyVariant Identifiers: chr7:g.151845806A>C (hg19) ; chr7:g.152148721A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.152148721A>C , CM000669.2:g.152148721A>C	GRCh38
NC_000007.13:g.151845806A>C , CM000669.1:g.151845806A>C	GRCh37
NC_000007.12:g.151476739A>C	NCBI36
NG_033948.1:g.292285T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682040.1:c.1394T>G
ENST00000682116.1:n.2338T>G
ENST00000682283.1:c.13377T>G	ENSP00000507485.1:p.Cys4459Trp
ENST00000682629.1:n.2506T>G
ENST00000683120.1:n.8398T>G
ENST00000683178.1:c.3779T>G
ENST00000683200.1:c.10716T>G	ENSP00000508052.1:p.Cys3572Trp
ENST00000683337.1:n.4836T>G
ENST00000683502.1:c.3851T>G
ENST00000683621.1:n.1972T>G
ENST00000683640.1:n.1922T>G
ENST00000684069.1:c.1623T>G	ENSP00000507650.1:p.Cys541Trp
ENST00000684261.1:c.8103T>G	ENSP00000508097.1:p.Cys2701Trp
ENST00000684649.1:c.3851T>G
ENST00000262189.11:c.13206T>G MANE Select	ENSP00000262189.6:p.Cys4402Trp
ENST00000360104.8:c.8993T>G
ENST00000418061.2:c.3848T>G
ENST00000424877.6:c.3782T>G
ENST00000679393.1:n.7917T>G
ENST00000679560.1:c.8106T>G	ENSP00000505094.1:p.Cys2702Trp
ENST00000679882.1:c.12771T>G	ENSP00000506154.1:p.Cys4257Trp
ENST00000680029.1:c.3783T>G
ENST00000680877.1:c.8106T>G	ENSP00000505724.1:p.Cys2702Trp
ENST00000681923.1:n.2221T>G
ENST00000262189.10:c.13206T>G	ENSP00000262189.6:p.Cys4402Trp
ENST00000355193.6:c.13206T>G	ENSP00000347325.3:p.Cys4402Trp
ENST00000360104.7:c.5887T>G
ENST00000424877.5:c.3057T>G	ENSP00000410411.1:p.Cys1019Trp
ENST00000473186.5:n.11088T>G
ENST00000558084.5:c.*10726T>G	ENSP00000453752.1:n.*10726T>G
NM_170606.2:c.13206T>G	NP_733751.2:p.Cys4402Trp
XM_005250025.3:c.13422T>G	XP_005250082.1:p.Cys4474Trp
XM_005250026.2:c.13419T>G	XP_005250083.1:p.Cys4473Trp
XM_005250027.3:c.13419T>G	XP_005250084.1:p.Cys4473Trp
XM_005250028.3:c.13422T>G	XP_005250085.1:p.Cys4474Trp
XM_005250031.3:c.13257T>G	XP_005250088.1:p.Cys4419Trp
XM_006716077.2:c.13419T>G	XP_006716140.1:p.Cys4473Trp
XM_006716078.2:c.13350T>G	XP_006716141.1:p.Cys4450Trp
XM_006716079.2:c.13254T>G	XP_006716142.1:p.Cys4418Trp
XM_011516450.1:c.13374T>G	XP_011514752.1:p.Cys4458Trp
XM_011516451.1:c.13302T>G	XP_011514753.1:p.Cys4434Trp
XM_011516452.1:c.13269T>G	XP_011514754.1:p.Cys4423Trp
XM_011516453.1:c.13185T>G	XP_011514755.1:p.Cys4395Trp
XM_011516454.1:c.12507T>G	XP_011514756.1:p.Cys4169Trp
XM_011516455.1:c.10968T>G	XP_011514757.1:p.Cys3656Trp
XM_011516456.1:c.13374T>G	XP_011514758.1:p.Cys4458Trp
XM_005250025.4:c.13422T>G	XP_005250082.1:p.Cys4474Trp
XM_005250026.3:c.13419T>G	XP_005250083.1:p.Cys4473Trp
XM_005250027.4:c.13419T>G	XP_005250084.1:p.Cys4473Trp
XM_005250028.4:c.13422T>G	XP_005250085.1:p.Cys4474Trp
XM_005250031.4:c.13257T>G	XP_005250088.1:p.Cys4419Trp
XM_006716077.3:c.13419T>G	XP_006716140.1:p.Cys4473Trp
XM_006716078.3:c.13350T>G	XP_006716141.1:p.Cys4450Trp
XM_006716079.3:c.13254T>G	XP_006716142.1:p.Cys4418Trp
XM_011516450.2:c.13374T>G	XP_011514752.1:p.Cys4458Trp
XM_011516451.2:c.13302T>G	XP_011514753.1:p.Cys4434Trp
XM_011516452.2:c.13269T>G	XP_011514754.1:p.Cys4423Trp
XM_011516453.2:c.13185T>G	XP_011514755.1:p.Cys4395Trp
XM_011516454.2:c.12507T>G	XP_011514756.1:p.Cys4169Trp
XM_011516456.2:c.13374T>G	XP_011514758.1:p.Cys4458Trp
XM_017012480.1:c.13422T>G	XP_016867969.1:p.Cys4474Trp
XM_017012481.1:c.13419T>G	XP_016867970.1:p.Cys4473Trp
XM_017012482.1:c.13419T>G	XP_016867971.1:p.Cys4473Trp
XM_017012483.1:c.13419T>G	XP_016867972.1:p.Cys4473Trp
XM_017012484.1:c.13389T>G	XP_016867973.1:p.Cys4463Trp
XM_017012485.1:c.13371T>G	XP_016867974.1:p.Cys4457Trp
XM_017012486.1:c.13347T>G	XP_016867975.1:p.Cys4449Trp
XM_017012487.1:c.13275T>G	XP_016867976.1:p.Cys4425Trp
XM_017012488.1:c.13239T>G	XP_016867977.1:p.Cys4413Trp
XM_017012489.1:c.10092T>G	XP_016867978.1:p.Cys3364Trp
XM_017012490.2:c.9696T>G	XP_016867979.1:p.Cys3232Trp
XM_024446852.1:c.13419T>G	XP_024302620.1:p.Cys4473Trp
XM_024446853.1:c.13347T>G	XP_024302621.1:p.Cys4449Trp
NM_170606.3:c.13206T>G MANE Select	NP_733751.2:p.Cys4402Trp