Canonical Allele Identifier: CA370093277

Gene: KMT2C

Linked Data

• MyVariant Identifiers: chr7:g.151845939T>C (hg19) ; chr7:g.152148854T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.152148854T>C , CM000669.2:g.152148854T>C	GRCh38
NC_000007.13:g.151845939T>C , CM000669.1:g.151845939T>C	GRCh37
NC_000007.12:g.151476872T>C	NCBI36
NG_033948.1:g.292152A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682040.1:c.1261A>G
ENST00000682116.1:n.2205A>G
ENST00000682283.1:c.13244A>G	ENSP00000507485.1:p.Lys4415Arg
ENST00000682629.1:n.2373A>G
ENST00000683120.1:n.8265A>G
ENST00000683178.1:c.3646A>G
ENST00000683200.1:c.10583A>G	ENSP00000508052.1:p.Lys3528Arg
ENST00000683337.1:n.4703A>G
ENST00000683502.1:c.3718A>G
ENST00000683621.1:n.1839A>G
ENST00000683640.1:n.1789A>G
ENST00000684069.1:c.1490A>G	ENSP00000507650.1:p.Lys497Arg
ENST00000684261.1:c.7970A>G	ENSP00000508097.1:p.Lys2657Arg
ENST00000684649.1:c.3718A>G
ENST00000262189.11:c.13073A>G MANE Select	ENSP00000262189.6:p.Lys4358Arg
ENST00000360104.8:c.8860A>G
ENST00000418061.2:c.3715A>G
ENST00000424877.6:c.3649A>G
ENST00000679393.1:n.7784A>G
ENST00000679560.1:c.7973A>G	ENSP00000505094.1:p.Lys2658Arg
ENST00000679882.1:c.12638A>G	ENSP00000506154.1:p.Lys4213Arg
ENST00000680029.1:c.3650A>G
ENST00000680877.1:c.7973A>G	ENSP00000505724.1:p.Lys2658Arg
ENST00000681923.1:n.2088A>G
ENST00000262189.10:c.13073A>G	ENSP00000262189.6:p.Lys4358Arg
ENST00000355193.6:c.13073A>G	ENSP00000347325.3:p.Lys4358Arg
ENST00000360104.7:c.5754A>G
ENST00000424877.5:c.2924A>G	ENSP00000410411.1:p.Lys975Arg
ENST00000473186.5:n.10955A>G
ENST00000558084.5:c.*10593A>G	ENSP00000453752.1:n.*10593A>G
NM_170606.2:c.13073A>G	NP_733751.2:p.Lys4358Arg
XM_005250025.3:c.13289A>G	XP_005250082.1:p.Lys4430Arg
XM_005250026.2:c.13286A>G	XP_005250083.1:p.Lys4429Arg
XM_005250027.3:c.13286A>G	XP_005250084.1:p.Lys4429Arg
XM_005250028.3:c.13289A>G	XP_005250085.1:p.Lys4430Arg
XM_005250031.3:c.13124A>G	XP_005250088.1:p.Lys4375Arg
XM_006716077.2:c.13286A>G	XP_006716140.1:p.Lys4429Arg
XM_006716078.2:c.13217A>G	XP_006716141.1:p.Lys4406Arg
XM_006716079.2:c.13121A>G	XP_006716142.1:p.Lys4374Arg
XM_011516450.1:c.13241A>G	XP_011514752.1:p.Lys4414Arg
XM_011516451.1:c.13169A>G	XP_011514753.1:p.Lys4390Arg
XM_011516452.1:c.13136A>G	XP_011514754.1:p.Lys4379Arg
XM_011516453.1:c.13052A>G	XP_011514755.1:p.Lys4351Arg
XM_011516454.1:c.12374A>G	XP_011514756.1:p.Lys4125Arg
XM_011516455.1:c.10835A>G	XP_011514757.1:p.Lys3612Arg
XM_011516456.1:c.13241A>G	XP_011514758.1:p.Lys4414Arg
XM_005250025.4:c.13289A>G	XP_005250082.1:p.Lys4430Arg
XM_005250026.3:c.13286A>G	XP_005250083.1:p.Lys4429Arg
XM_005250027.4:c.13286A>G	XP_005250084.1:p.Lys4429Arg
XM_005250028.4:c.13289A>G	XP_005250085.1:p.Lys4430Arg
XM_005250031.4:c.13124A>G	XP_005250088.1:p.Lys4375Arg
XM_006716077.3:c.13286A>G	XP_006716140.1:p.Lys4429Arg
XM_006716078.3:c.13217A>G	XP_006716141.1:p.Lys4406Arg
XM_006716079.3:c.13121A>G	XP_006716142.1:p.Lys4374Arg
XM_011516450.2:c.13241A>G	XP_011514752.1:p.Lys4414Arg
XM_011516451.2:c.13169A>G	XP_011514753.1:p.Lys4390Arg
XM_011516452.2:c.13136A>G	XP_011514754.1:p.Lys4379Arg
XM_011516453.2:c.13052A>G	XP_011514755.1:p.Lys4351Arg
XM_011516454.2:c.12374A>G	XP_011514756.1:p.Lys4125Arg
XM_011516456.2:c.13241A>G	XP_011514758.1:p.Lys4414Arg
XM_017012480.1:c.13289A>G	XP_016867969.1:p.Lys4430Arg
XM_017012481.1:c.13286A>G	XP_016867970.1:p.Lys4429Arg
XM_017012482.1:c.13286A>G	XP_016867971.1:p.Lys4429Arg
XM_017012483.1:c.13286A>G	XP_016867972.1:p.Lys4429Arg
XM_017012484.1:c.13256A>G	XP_016867973.1:p.Lys4419Arg
XM_017012485.1:c.13238A>G	XP_016867974.1:p.Lys4413Arg
XM_017012486.1:c.13214A>G	XP_016867975.1:p.Lys4405Arg
XM_017012487.1:c.13142A>G	XP_016867976.1:p.Lys4381Arg
XM_017012488.1:c.13106A>G	XP_016867977.1:p.Lys4369Arg
XM_017012489.1:c.9959A>G	XP_016867978.1:p.Lys3320Arg
XM_017012490.2:c.9563A>G	XP_016867979.1:p.Lys3188Arg
XM_024446852.1:c.13286A>G	XP_024302620.1:p.Lys4429Arg
XM_024446853.1:c.13214A>G	XP_024302621.1:p.Lys4405Arg
NM_170606.3:c.13073A>G MANE Select	NP_733751.2:p.Lys4358Arg