Canonical Allele Identifier: CA370100547

Gene: KMT2C

Linked Data

• dbSNP Id: rs2129121630
• gnomAD v4: 7-152183149-G-A
• MyVariant Identifiers: chr7:g.151880234G>A (hg19) ; chr7:g.152183149G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.152183149G>A , CM000669.2:g.152183149G>A	GRCh38
NC_000007.13:g.151880234G>A , CM000669.1:g.151880234G>A	GRCh37
NC_000007.12:g.151511167G>A	NCBI36
NG_033948.1:g.257857C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682176.1:c.1809C>T
ENST00000682283.1:c.5090C>T	ENSP00000507485.1:p.Ala1697Val
ENST00000683159.1:c.576-555C>T
ENST00000683200.1:c.2438C>T	ENSP00000508052.1:p.Ala813Val
ENST00000262189.11:c.5090C>T MANE Select	ENSP00000262189.6:p.Ala1697Val
ENST00000360104.8:c.712C>T
ENST00000679645.1:c.*1183C>T	ENSP00000505745.1:n.*1183C>T
ENST00000679882.1:c.4865C>T	ENSP00000506154.1:p.Ala1622Val
ENST00000680969.1:c.2486C>T	ENSP00000505951.1:p.Ala829Val
ENST00000681033.1:c.3788C>T	ENSP00000505058.1:p.Ala1263Val
ENST00000681755.1:n.15C>T
ENST00000262189.10:c.5090C>T	ENSP00000262189.6:p.Ala1697Val
ENST00000355193.6:c.5090C>T	ENSP00000347325.3:p.Ala1697Val
ENST00000473186.5:n.2801C>T
ENST00000558084.5:c.*2610C>T	ENSP00000453752.1:n.*2610C>T
NM_170606.2:c.5090C>T	NP_733751.2:p.Ala1697Val
XM_005250025.3:c.5141C>T	XP_005250082.1:p.Ala1714Val
XM_005250026.2:c.5138C>T	XP_005250083.1:p.Ala1713Val
XM_005250027.3:c.5141C>T	XP_005250084.1:p.Ala1714Val
XM_005250028.3:c.5141C>T	XP_005250085.1:p.Ala1714Val
XM_005250031.3:c.5141C>T	XP_005250088.1:p.Ala1714Val
XM_006716077.2:c.5141C>T	XP_006716140.1:p.Ala1714Val
XM_006716078.2:c.5141C>T	XP_006716141.1:p.Ala1714Val
XM_006716079.2:c.5141C>T	XP_006716142.1:p.Ala1714Val
XM_011516450.1:c.5093C>T	XP_011514752.1:p.Ala1698Val
XM_011516451.1:c.5021C>T	XP_011514753.1:p.Ala1674Val
XM_011516452.1:c.4988C>T	XP_011514754.1:p.Ala1663Val
XM_011516453.1:c.5141C>T	XP_011514755.1:p.Ala1714Val
XM_011516454.1:c.4226C>T	XP_011514756.1:p.Ala1409Val
XM_011516455.1:c.2687C>T	XP_011514757.1:p.Ala896Val
XM_011516456.1:c.5093C>T	XP_011514758.1:p.Ala1698Val
XR_428183.2:n.5349C>T
XM_005250025.4:c.5141C>T	XP_005250082.1:p.Ala1714Val
XM_005250026.3:c.5138C>T	XP_005250083.1:p.Ala1713Val
XM_005250027.4:c.5141C>T	XP_005250084.1:p.Ala1714Val
XM_005250028.4:c.5141C>T	XP_005250085.1:p.Ala1714Val
XM_005250031.4:c.5141C>T	XP_005250088.1:p.Ala1714Val
XM_006716077.3:c.5141C>T	XP_006716140.1:p.Ala1714Val
XM_006716078.3:c.5141C>T	XP_006716141.1:p.Ala1714Val
XM_006716079.3:c.5141C>T	XP_006716142.1:p.Ala1714Val
XM_011516450.2:c.5093C>T	XP_011514752.1:p.Ala1698Val
XM_011516451.2:c.5021C>T	XP_011514753.1:p.Ala1674Val
XM_011516452.2:c.4988C>T	XP_011514754.1:p.Ala1663Val
XM_011516453.2:c.5141C>T	XP_011514755.1:p.Ala1714Val
XM_011516454.2:c.4226C>T	XP_011514756.1:p.Ala1409Val
XM_011516456.2:c.5093C>T	XP_011514758.1:p.Ala1698Val
XM_017012480.1:c.5141C>T	XP_016867969.1:p.Ala1714Val
XM_017012481.1:c.5138C>T	XP_016867970.1:p.Ala1713Val
XM_017012482.1:c.5141C>T	XP_016867971.1:p.Ala1714Val
XM_017012483.1:c.5141C>T	XP_016867972.1:p.Ala1714Val
XM_017012484.1:c.5108C>T	XP_016867973.1:p.Ala1703Val
XM_017012485.1:c.5090C>T	XP_016867974.1:p.Ala1697Val
XM_017012486.1:c.5141C>T	XP_016867975.1:p.Ala1714Val
XM_017012487.1:c.4994C>T	XP_016867976.1:p.Ala1665Val
XM_017012488.1:c.5134-555C>T	XP_016867977.1:n.5134-555C>T
XM_017012489.1:c.1811C>T	XP_016867978.1:p.Ala604Val
XM_017012490.2:c.1415C>T	XP_016867979.1:p.Ala472Val
XM_024446852.1:c.5138C>T	XP_024302620.1:p.Ala1713Val
XM_024446853.1:c.5141C>T	XP_024302621.1:p.Ala1714Val
XR_428183.3:n.5373C>T
NM_170606.3:c.5090C>T MANE Select	NP_733751.2:p.Ala1697Val