Canonical Allele Identifier: CA375793713

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140707610A>G (hg19) ; chr9:g.137813158A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137813158A>G , CM000671.2:g.137813158A>G	GRCh38
NC_000009.11:g.140707610A>G , CM000671.1:g.140707610A>G	GRCh37
NC_000009.10:g.139827431A>G	NCBI36
NG_011776.1:g.199167A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.3020A>G MANE Select	ENSP00000417980.1:p.Glu1007Gly
ENST00000636027.1:c.2906A>G	ENSP00000489961.1:p.Glu969Gly
ENST00000637161.1:c.2927A>G	ENSP00000490328.1:p.Glu976Gly
ENST00000637261.1:c.3060A>G	ENSP00000490815.1:n.3060A>G
ENST00000637891.1:c.914A>G	ENSP00000490907.1:p.Glu305Gly
ENST00000460843.5:c.3020A>G	ENSP00000417980.1:p.Glu1007Gly
ENST00000462942.3:c.1877A>G	ENSP00000436107.1:p.Glu626Gly
ENST00000486164.5:c.707A>G
ENST00000488242.2:n.546A>G
NM_024757.4:c.3020A>G	NP_079033.4:p.Glu1007Gly
XM_005266105.3:c.3011A>G	XP_005266162.1:p.Glu1004Gly
XM_005266110.1:c.2927A>G	XP_005266167.1:p.Glu976Gly
XM_006717288.2:c.3002A>G	XP_006717351.1:p.Glu1001Gly
XM_011519021.1:c.3029A>G	XP_011517323.1:p.Glu1010Gly
XM_011519022.1:c.3026A>G	XP_011517324.1:p.Glu1009Gly
XM_011519023.1:c.3008A>G	XP_011517325.1:p.Glu1003Gly
XM_011519024.1:c.2951A>G	XP_011517326.1:p.Glu984Gly
XM_011519025.1:c.2927A>G	XP_011517327.1:p.Glu976Gly
XM_011519026.1:c.2885A>G	XP_011517328.1:p.Glu962Gly
XM_011519029.1:c.1451A>G	XP_011517331.1:p.Glu484Gly
XM_011519030.1:c.803A>G	XP_011517332.1:p.Glu268Gly
XM_011519031.1:c.590A>G	XP_011517333.1:p.Glu197Gly
XM_011519032.1:c.590A>G	XP_011517334.1:p.Glu197Gly
XM_011519033.1:c.2864A>G	XP_011517335.1:p.Glu955Gly
NM_001354263.1:c.2999A>G	NP_001341192.1:p.Glu1000Gly
XM_005266105.5:c.3011A>G	XP_005266162.1:p.Glu1004Gly
XM_011519021.3:c.3029A>G	XP_011517323.1:p.Glu1010Gly
XM_011519022.3:c.3026A>G	XP_011517324.1:p.Glu1009Gly
XM_011519023.3:c.3008A>G	XP_011517325.1:p.Glu1003Gly
XM_011519029.3:c.1451A>G	XP_011517331.1:p.Glu484Gly
XM_011519030.3:c.803A>G	XP_011517332.1:p.Glu268Gly
XM_017015134.1:c.3005A>G	XP_016870623.1:p.Glu1002Gly
XM_017015136.2:c.2921A>G	XP_016870625.1:p.Glu974Gly
XM_017015137.1:c.2906A>G	XP_016870626.1:p.Glu969Gly
XM_017015138.1:c.2906A>G	XP_016870627.1:p.Glu969Gly
XM_024447674.1:c.2849A>G	XP_024303442.1:p.Glu950Gly
XM_024447675.1:c.2783A>G	XP_024303443.1:p.Glu928Gly
XM_024447676.1:c.2144A>G	XP_024303444.1:p.Glu715Gly
XM_024447677.1:c.2144A>G	XP_024303445.1:p.Glu715Gly
XM_024447680.1:c.2762A>G	XP_024303448.1:p.Glu921Gly
NM_024757.5:c.3020A>G MANE Select	NP_079033.4:p.Glu1007Gly
NM_001354263.2:c.2999A>G	NP_001341192.1:p.Glu1000Gly