Canonical Allele Identifier: CA370093053

Gene: KMT2C

Linked Data

• MyVariant Identifiers: chr7:g.151845874C>T (hg19) ; chr7:g.152148789C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.152148789C>T , CM000669.2:g.152148789C>T	GRCh38
NC_000007.13:g.151845874C>T , CM000669.1:g.151845874C>T	GRCh37
NC_000007.12:g.151476807C>T	NCBI36
NG_033948.1:g.292217G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682040.1:c.1326G>A
ENST00000682116.1:n.2270G>A
ENST00000682283.1:c.13309G>A	ENSP00000507485.1:p.Asp4437Asn
ENST00000682629.1:n.2438G>A
ENST00000683120.1:n.8330G>A
ENST00000683178.1:c.3711G>A
ENST00000683200.1:c.10648G>A	ENSP00000508052.1:p.Asp3550Asn
ENST00000683337.1:n.4768G>A
ENST00000683502.1:c.3783G>A
ENST00000683621.1:n.1904G>A
ENST00000683640.1:n.1854G>A
ENST00000684069.1:c.1555G>A	ENSP00000507650.1:p.Asp519Asn
ENST00000684261.1:c.8035G>A	ENSP00000508097.1:p.Asp2679Asn
ENST00000684649.1:c.3783G>A
ENST00000262189.11:c.13138G>A MANE Select	ENSP00000262189.6:p.Asp4380Asn
ENST00000360104.8:c.8925G>A
ENST00000418061.2:c.3780G>A
ENST00000424877.6:c.3714G>A
ENST00000679393.1:n.7849G>A
ENST00000679560.1:c.8038G>A	ENSP00000505094.1:p.Asp2680Asn
ENST00000679882.1:c.12703G>A	ENSP00000506154.1:p.Asp4235Asn
ENST00000680029.1:c.3715G>A
ENST00000680877.1:c.8038G>A	ENSP00000505724.1:p.Asp2680Asn
ENST00000681923.1:n.2153G>A
ENST00000262189.10:c.13138G>A	ENSP00000262189.6:p.Asp4380Asn
ENST00000355193.6:c.13138G>A	ENSP00000347325.3:p.Asp4380Asn
ENST00000360104.7:c.5819G>A
ENST00000424877.5:c.2989G>A	ENSP00000410411.1:p.Asp997Asn
ENST00000473186.5:n.11020G>A
ENST00000558084.5:c.*10658G>A	ENSP00000453752.1:n.*10658G>A
NM_170606.2:c.13138G>A	NP_733751.2:p.Asp4380Asn
XM_005250025.3:c.13354G>A	XP_005250082.1:p.Asp4452Asn
XM_005250026.2:c.13351G>A	XP_005250083.1:p.Asp4451Asn
XM_005250027.3:c.13351G>A	XP_005250084.1:p.Asp4451Asn
XM_005250028.3:c.13354G>A	XP_005250085.1:p.Asp4452Asn
XM_005250031.3:c.13189G>A	XP_005250088.1:p.Asp4397Asn
XM_006716077.2:c.13351G>A	XP_006716140.1:p.Asp4451Asn
XM_006716078.2:c.13282G>A	XP_006716141.1:p.Asp4428Asn
XM_006716079.2:c.13186G>A	XP_006716142.1:p.Asp4396Asn
XM_011516450.1:c.13306G>A	XP_011514752.1:p.Asp4436Asn
XM_011516451.1:c.13234G>A	XP_011514753.1:p.Asp4412Asn
XM_011516452.1:c.13201G>A	XP_011514754.1:p.Asp4401Asn
XM_011516453.1:c.13117G>A	XP_011514755.1:p.Asp4373Asn
XM_011516454.1:c.12439G>A	XP_011514756.1:p.Asp4147Asn
XM_011516455.1:c.10900G>A	XP_011514757.1:p.Asp3634Asn
XM_011516456.1:c.13306G>A	XP_011514758.1:p.Asp4436Asn
XM_005250025.4:c.13354G>A	XP_005250082.1:p.Asp4452Asn
XM_005250026.3:c.13351G>A	XP_005250083.1:p.Asp4451Asn
XM_005250027.4:c.13351G>A	XP_005250084.1:p.Asp4451Asn
XM_005250028.4:c.13354G>A	XP_005250085.1:p.Asp4452Asn
XM_005250031.4:c.13189G>A	XP_005250088.1:p.Asp4397Asn
XM_006716077.3:c.13351G>A	XP_006716140.1:p.Asp4451Asn
XM_006716078.3:c.13282G>A	XP_006716141.1:p.Asp4428Asn
XM_006716079.3:c.13186G>A	XP_006716142.1:p.Asp4396Asn
XM_011516450.2:c.13306G>A	XP_011514752.1:p.Asp4436Asn
XM_011516451.2:c.13234G>A	XP_011514753.1:p.Asp4412Asn
XM_011516452.2:c.13201G>A	XP_011514754.1:p.Asp4401Asn
XM_011516453.2:c.13117G>A	XP_011514755.1:p.Asp4373Asn
XM_011516454.2:c.12439G>A	XP_011514756.1:p.Asp4147Asn
XM_011516456.2:c.13306G>A	XP_011514758.1:p.Asp4436Asn
XM_017012480.1:c.13354G>A	XP_016867969.1:p.Asp4452Asn
XM_017012481.1:c.13351G>A	XP_016867970.1:p.Asp4451Asn
XM_017012482.1:c.13351G>A	XP_016867971.1:p.Asp4451Asn
XM_017012483.1:c.13351G>A	XP_016867972.1:p.Asp4451Asn
XM_017012484.1:c.13321G>A	XP_016867973.1:p.Asp4441Asn
XM_017012485.1:c.13303G>A	XP_016867974.1:p.Asp4435Asn
XM_017012486.1:c.13279G>A	XP_016867975.1:p.Asp4427Asn
XM_017012487.1:c.13207G>A	XP_016867976.1:p.Asp4403Asn
XM_017012488.1:c.13171G>A	XP_016867977.1:p.Asp4391Asn
XM_017012489.1:c.10024G>A	XP_016867978.1:p.Asp3342Asn
XM_017012490.2:c.9628G>A	XP_016867979.1:p.Asp3210Asn
XM_024446852.1:c.13351G>A	XP_024302620.1:p.Asp4451Asn
XM_024446853.1:c.13279G>A	XP_024302621.1:p.Asp4427Asn
NM_170606.3:c.13138G>A MANE Select	NP_733751.2:p.Asp4380Asn