Canonical Allele Identifier: CA370093084

Gene: KMT2C

Linked Data

• MyVariant Identifiers: chr7:g.151845882T>C (hg19) ; chr7:g.152148797T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.152148797T>C , CM000669.2:g.152148797T>C	GRCh38
NC_000007.13:g.151845882T>C , CM000669.1:g.151845882T>C	GRCh37
NC_000007.12:g.151476815T>C	NCBI36
NG_033948.1:g.292209A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682040.1:c.1318A>G
ENST00000682116.1:n.2262A>G
ENST00000682283.1:c.13301A>G	ENSP00000507485.1:p.Asp4434Gly
ENST00000682629.1:n.2430A>G
ENST00000683120.1:n.8322A>G
ENST00000683178.1:c.3703A>G
ENST00000683200.1:c.10640A>G	ENSP00000508052.1:p.Asp3547Gly
ENST00000683337.1:n.4760A>G
ENST00000683502.1:c.3775A>G
ENST00000683621.1:n.1896A>G
ENST00000683640.1:n.1846A>G
ENST00000684069.1:c.1547A>G	ENSP00000507650.1:p.Asp516Gly
ENST00000684261.1:c.8027A>G	ENSP00000508097.1:p.Asp2676Gly
ENST00000684649.1:c.3775A>G
ENST00000262189.11:c.13130A>G MANE Select	ENSP00000262189.6:p.Asp4377Gly
ENST00000360104.8:c.8917A>G
ENST00000418061.2:c.3772A>G
ENST00000424877.6:c.3706A>G
ENST00000679393.1:n.7841A>G
ENST00000679560.1:c.8030A>G	ENSP00000505094.1:p.Asp2677Gly
ENST00000679882.1:c.12695A>G	ENSP00000506154.1:p.Asp4232Gly
ENST00000680029.1:c.3707A>G
ENST00000680877.1:c.8030A>G	ENSP00000505724.1:p.Asp2677Gly
ENST00000681923.1:n.2145A>G
ENST00000262189.10:c.13130A>G	ENSP00000262189.6:p.Asp4377Gly
ENST00000355193.6:c.13130A>G	ENSP00000347325.3:p.Asp4377Gly
ENST00000360104.7:c.5811A>G
ENST00000424877.5:c.2981A>G	ENSP00000410411.1:p.Asp994Gly
ENST00000473186.5:n.11012A>G
ENST00000558084.5:c.*10650A>G	ENSP00000453752.1:n.*10650A>G
NM_170606.2:c.13130A>G	NP_733751.2:p.Asp4377Gly
XM_005250025.3:c.13346A>G	XP_005250082.1:p.Asp4449Gly
XM_005250026.2:c.13343A>G	XP_005250083.1:p.Asp4448Gly
XM_005250027.3:c.13343A>G	XP_005250084.1:p.Asp4448Gly
XM_005250028.3:c.13346A>G	XP_005250085.1:p.Asp4449Gly
XM_005250031.3:c.13181A>G	XP_005250088.1:p.Asp4394Gly
XM_006716077.2:c.13343A>G	XP_006716140.1:p.Asp4448Gly
XM_006716078.2:c.13274A>G	XP_006716141.1:p.Asp4425Gly
XM_006716079.2:c.13178A>G	XP_006716142.1:p.Asp4393Gly
XM_011516450.1:c.13298A>G	XP_011514752.1:p.Asp4433Gly
XM_011516451.1:c.13226A>G	XP_011514753.1:p.Asp4409Gly
XM_011516452.1:c.13193A>G	XP_011514754.1:p.Asp4398Gly
XM_011516453.1:c.13109A>G	XP_011514755.1:p.Asp4370Gly
XM_011516454.1:c.12431A>G	XP_011514756.1:p.Asp4144Gly
XM_011516455.1:c.10892A>G	XP_011514757.1:p.Asp3631Gly
XM_011516456.1:c.13298A>G	XP_011514758.1:p.Asp4433Gly
XM_005250025.4:c.13346A>G	XP_005250082.1:p.Asp4449Gly
XM_005250026.3:c.13343A>G	XP_005250083.1:p.Asp4448Gly
XM_005250027.4:c.13343A>G	XP_005250084.1:p.Asp4448Gly
XM_005250028.4:c.13346A>G	XP_005250085.1:p.Asp4449Gly
XM_005250031.4:c.13181A>G	XP_005250088.1:p.Asp4394Gly
XM_006716077.3:c.13343A>G	XP_006716140.1:p.Asp4448Gly
XM_006716078.3:c.13274A>G	XP_006716141.1:p.Asp4425Gly
XM_006716079.3:c.13178A>G	XP_006716142.1:p.Asp4393Gly
XM_011516450.2:c.13298A>G	XP_011514752.1:p.Asp4433Gly
XM_011516451.2:c.13226A>G	XP_011514753.1:p.Asp4409Gly
XM_011516452.2:c.13193A>G	XP_011514754.1:p.Asp4398Gly
XM_011516453.2:c.13109A>G	XP_011514755.1:p.Asp4370Gly
XM_011516454.2:c.12431A>G	XP_011514756.1:p.Asp4144Gly
XM_011516456.2:c.13298A>G	XP_011514758.1:p.Asp4433Gly
XM_017012480.1:c.13346A>G	XP_016867969.1:p.Asp4449Gly
XM_017012481.1:c.13343A>G	XP_016867970.1:p.Asp4448Gly
XM_017012482.1:c.13343A>G	XP_016867971.1:p.Asp4448Gly
XM_017012483.1:c.13343A>G	XP_016867972.1:p.Asp4448Gly
XM_017012484.1:c.13313A>G	XP_016867973.1:p.Asp4438Gly
XM_017012485.1:c.13295A>G	XP_016867974.1:p.Asp4432Gly
XM_017012486.1:c.13271A>G	XP_016867975.1:p.Asp4424Gly
XM_017012487.1:c.13199A>G	XP_016867976.1:p.Asp4400Gly
XM_017012488.1:c.13163A>G	XP_016867977.1:p.Asp4388Gly
XM_017012489.1:c.10016A>G	XP_016867978.1:p.Asp3339Gly
XM_017012490.2:c.9620A>G	XP_016867979.1:p.Asp3207Gly
XM_024446852.1:c.13343A>G	XP_024302620.1:p.Asp4448Gly
XM_024446853.1:c.13271A>G	XP_024302621.1:p.Asp4424Gly
NM_170606.3:c.13130A>G MANE Select	NP_733751.2:p.Asp4377Gly