Canonical Allele Identifier: CA370091914

Gene: KMT2C

Linked Data

• dbSNP Id: rs2129095496
• MyVariant Identifiers: chr7:g.151845781C>T (hg19) ; chr7:g.152148696C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.152148696C>T , CM000669.2:g.152148696C>T	GRCh38
NC_000007.13:g.151845781C>T , CM000669.1:g.151845781C>T	GRCh37
NC_000007.12:g.151476714C>T	NCBI36
NG_033948.1:g.292310G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682040.1:c.1419G>A
ENST00000682116.1:n.2363G>A
ENST00000682283.1:c.13402G>A	ENSP00000507485.1:p.Gly4468Arg
ENST00000682629.1:n.2531G>A
ENST00000683120.1:n.8423G>A
ENST00000683178.1:c.3804G>A
ENST00000683200.1:c.10741G>A	ENSP00000508052.1:p.Gly3581Arg
ENST00000683337.1:n.4861G>A
ENST00000683502.1:c.3876G>A
ENST00000683621.1:n.1997G>A
ENST00000683640.1:n.1947G>A
ENST00000684069.1:c.1648G>A	ENSP00000507650.1:p.Gly550Arg
ENST00000684261.1:c.8128G>A	ENSP00000508097.1:p.Gly2710Arg
ENST00000684649.1:c.3876G>A
ENST00000262189.11:c.13231G>A MANE Select	ENSP00000262189.6:p.Gly4411Arg
ENST00000360104.8:c.9018G>A
ENST00000418061.2:c.3873G>A
ENST00000424877.6:c.3807G>A
ENST00000679393.1:n.7942G>A
ENST00000679560.1:c.8131G>A	ENSP00000505094.1:p.Gly2711Arg
ENST00000679882.1:c.12796G>A	ENSP00000506154.1:p.Gly4266Arg
ENST00000680029.1:c.3808G>A
ENST00000680877.1:c.8131G>A	ENSP00000505724.1:p.Gly2711Arg
ENST00000681923.1:n.2246G>A
ENST00000262189.10:c.13231G>A	ENSP00000262189.6:p.Gly4411Arg
ENST00000355193.6:c.13231G>A	ENSP00000347325.3:p.Gly4411Arg
ENST00000360104.7:c.5912G>A
ENST00000424877.5:c.3082G>A	ENSP00000410411.1:p.Gly1028Arg
ENST00000473186.5:n.11113G>A
ENST00000558084.5:c.*10751G>A	ENSP00000453752.1:n.*10751G>A
NM_170606.2:c.13231G>A	NP_733751.2:p.Gly4411Arg
XM_005250025.3:c.13447G>A	XP_005250082.1:p.Gly4483Arg
XM_005250026.2:c.13444G>A	XP_005250083.1:p.Gly4482Arg
XM_005250027.3:c.13444G>A	XP_005250084.1:p.Gly4482Arg
XM_005250028.3:c.13447G>A	XP_005250085.1:p.Gly4483Arg
XM_005250031.3:c.13282G>A	XP_005250088.1:p.Gly4428Arg
XM_006716077.2:c.13444G>A	XP_006716140.1:p.Gly4482Arg
XM_006716078.2:c.13375G>A	XP_006716141.1:p.Gly4459Arg
XM_006716079.2:c.13279G>A	XP_006716142.1:p.Gly4427Arg
XM_011516450.1:c.13399G>A	XP_011514752.1:p.Gly4467Arg
XM_011516451.1:c.13327G>A	XP_011514753.1:p.Gly4443Arg
XM_011516452.1:c.13294G>A	XP_011514754.1:p.Gly4432Arg
XM_011516453.1:c.13210G>A	XP_011514755.1:p.Gly4404Arg
XM_011516454.1:c.12532G>A	XP_011514756.1:p.Gly4178Arg
XM_011516455.1:c.10993G>A	XP_011514757.1:p.Gly3665Arg
XM_011516456.1:c.13399G>A	XP_011514758.1:p.Gly4467Arg
XM_005250025.4:c.13447G>A	XP_005250082.1:p.Gly4483Arg
XM_005250026.3:c.13444G>A	XP_005250083.1:p.Gly4482Arg
XM_005250027.4:c.13444G>A	XP_005250084.1:p.Gly4482Arg
XM_005250028.4:c.13447G>A	XP_005250085.1:p.Gly4483Arg
XM_005250031.4:c.13282G>A	XP_005250088.1:p.Gly4428Arg
XM_006716077.3:c.13444G>A	XP_006716140.1:p.Gly4482Arg
XM_006716078.3:c.13375G>A	XP_006716141.1:p.Gly4459Arg
XM_006716079.3:c.13279G>A	XP_006716142.1:p.Gly4427Arg
XM_011516450.2:c.13399G>A	XP_011514752.1:p.Gly4467Arg
XM_011516451.2:c.13327G>A	XP_011514753.1:p.Gly4443Arg
XM_011516452.2:c.13294G>A	XP_011514754.1:p.Gly4432Arg
XM_011516453.2:c.13210G>A	XP_011514755.1:p.Gly4404Arg
XM_011516454.2:c.12532G>A	XP_011514756.1:p.Gly4178Arg
XM_011516456.2:c.13399G>A	XP_011514758.1:p.Gly4467Arg
XM_017012480.1:c.13447G>A	XP_016867969.1:p.Gly4483Arg
XM_017012481.1:c.13444G>A	XP_016867970.1:p.Gly4482Arg
XM_017012482.1:c.13444G>A	XP_016867971.1:p.Gly4482Arg
XM_017012483.1:c.13444G>A	XP_016867972.1:p.Gly4482Arg
XM_017012484.1:c.13414G>A	XP_016867973.1:p.Gly4472Arg
XM_017012485.1:c.13396G>A	XP_016867974.1:p.Gly4466Arg
XM_017012486.1:c.13372G>A	XP_016867975.1:p.Gly4458Arg
XM_017012487.1:c.13300G>A	XP_016867976.1:p.Gly4434Arg
XM_017012488.1:c.13264G>A	XP_016867977.1:p.Gly4422Arg
XM_017012489.1:c.10117G>A	XP_016867978.1:p.Gly3373Arg
XM_017012490.2:c.9721G>A	XP_016867979.1:p.Gly3241Arg
XM_024446852.1:c.13444G>A	XP_024302620.1:p.Gly4482Arg
XM_024446853.1:c.13372G>A	XP_024302621.1:p.Gly4458Arg
NM_170606.3:c.13231G>A MANE Select	NP_733751.2:p.Gly4411Arg