Canonical Allele Identifier: CA370100075

Gene: KMT2C

Linked Data

• MyVariant Identifiers: chr7:g.151880132A>C (hg19) ; chr7:g.152183047A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.152183047A>C , CM000669.2:g.152183047A>C	GRCh38
NC_000007.13:g.151880132A>C , CM000669.1:g.151880132A>C	GRCh37
NC_000007.12:g.151511065A>C	NCBI36
NG_033948.1:g.257959T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000682176.1:c.1911T>G
ENST00000682283.1:c.5192T>G	ENSP00000507485.1:p.Ile1731Ser
ENST00000683159.1:c.576-453T>G
ENST00000683200.1:c.2540T>G	ENSP00000508052.1:p.Ile847Ser
ENST00000262189.11:c.5192T>G MANE Select	ENSP00000262189.6:p.Ile1731Ser
ENST00000360104.8:c.814T>G
ENST00000679645.1:c.*1285T>G	ENSP00000505745.1:n.*1285T>G
ENST00000679882.1:c.4967T>G	ENSP00000506154.1:p.Ile1656Ser
ENST00000680969.1:c.2588T>G	ENSP00000505951.1:p.Ile863Ser
ENST00000681033.1:c.3890T>G	ENSP00000505058.1:p.Ile1297Ser
ENST00000681755.1:n.117T>G
ENST00000262189.10:c.5192T>G	ENSP00000262189.6:p.Ile1731Ser
ENST00000355193.6:c.5192T>G	ENSP00000347325.3:p.Ile1731Ser
ENST00000473186.5:n.2903T>G
ENST00000558084.5:c.*2712T>G	ENSP00000453752.1:n.*2712T>G
NM_170606.2:c.5192T>G	NP_733751.2:p.Ile1731Ser
XM_005250025.3:c.5243T>G	XP_005250082.1:p.Ile1748Ser
XM_005250026.2:c.5240T>G	XP_005250083.1:p.Ile1747Ser
XM_005250027.3:c.5243T>G	XP_005250084.1:p.Ile1748Ser
XM_005250028.3:c.5243T>G	XP_005250085.1:p.Ile1748Ser
XM_005250031.3:c.5243T>G	XP_005250088.1:p.Ile1748Ser
XM_006716077.2:c.5243T>G	XP_006716140.1:p.Ile1748Ser
XM_006716078.2:c.5243T>G	XP_006716141.1:p.Ile1748Ser
XM_006716079.2:c.5243T>G	XP_006716142.1:p.Ile1748Ser
XM_011516450.1:c.5195T>G	XP_011514752.1:p.Ile1732Ser
XM_011516451.1:c.5123T>G	XP_011514753.1:p.Ile1708Ser
XM_011516452.1:c.5090T>G	XP_011514754.1:p.Ile1697Ser
XM_011516453.1:c.5243T>G	XP_011514755.1:p.Ile1748Ser
XM_011516454.1:c.4328T>G	XP_011514756.1:p.Ile1443Ser
XM_011516455.1:c.2789T>G	XP_011514757.1:p.Ile930Ser
XM_011516456.1:c.5195T>G	XP_011514758.1:p.Ile1732Ser
XR_428183.2:n.5451T>G
XM_005250025.4:c.5243T>G	XP_005250082.1:p.Ile1748Ser
XM_005250026.3:c.5240T>G	XP_005250083.1:p.Ile1747Ser
XM_005250027.4:c.5243T>G	XP_005250084.1:p.Ile1748Ser
XM_005250028.4:c.5243T>G	XP_005250085.1:p.Ile1748Ser
XM_005250031.4:c.5243T>G	XP_005250088.1:p.Ile1748Ser
XM_006716077.3:c.5243T>G	XP_006716140.1:p.Ile1748Ser
XM_006716078.3:c.5243T>G	XP_006716141.1:p.Ile1748Ser
XM_006716079.3:c.5243T>G	XP_006716142.1:p.Ile1748Ser
XM_011516450.2:c.5195T>G	XP_011514752.1:p.Ile1732Ser
XM_011516451.2:c.5123T>G	XP_011514753.1:p.Ile1708Ser
XM_011516452.2:c.5090T>G	XP_011514754.1:p.Ile1697Ser
XM_011516453.2:c.5243T>G	XP_011514755.1:p.Ile1748Ser
XM_011516454.2:c.4328T>G	XP_011514756.1:p.Ile1443Ser
XM_011516456.2:c.5195T>G	XP_011514758.1:p.Ile1732Ser
XM_017012480.1:c.5243T>G	XP_016867969.1:p.Ile1748Ser
XM_017012481.1:c.5240T>G	XP_016867970.1:p.Ile1747Ser
XM_017012482.1:c.5243T>G	XP_016867971.1:p.Ile1748Ser
XM_017012483.1:c.5243T>G	XP_016867972.1:p.Ile1748Ser
XM_017012484.1:c.5210T>G	XP_016867973.1:p.Ile1737Ser
XM_017012485.1:c.5192T>G	XP_016867974.1:p.Ile1731Ser
XM_017012486.1:c.5243T>G	XP_016867975.1:p.Ile1748Ser
XM_017012487.1:c.5096T>G	XP_016867976.1:p.Ile1699Ser
XM_017012488.1:c.5134-453T>G	XP_016867977.1:n.5134-453T>G
XM_017012489.1:c.1913T>G	XP_016867978.1:p.Ile638Ser
XM_017012490.2:c.1517T>G	XP_016867979.1:p.Ile506Ser
XM_024446852.1:c.5240T>G	XP_024302620.1:p.Ile1747Ser
XM_024446853.1:c.5243T>G	XP_024302621.1:p.Ile1748Ser
XR_428183.3:n.5475T>G
NM_170606.3:c.5192T>G MANE Select	NP_733751.2:p.Ile1731Ser