Canonical Allele Identifier: CA375793712

Gene: EHMT1

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.3020A>C MANE Select	ENSP00000417980.1:p.Glu1007Ala
ENST00000636027.1:c.2906A>C	ENSP00000489961.1:p.Glu969Ala
ENST00000637161.1:c.2927A>C	ENSP00000490328.1:p.Glu976Ala
ENST00000637261.1:c.3060A>C	ENSP00000490815.1:n.3060A>C
ENST00000637891.1:c.914A>C	ENSP00000490907.1:p.Glu305Ala
ENST00000460843.5:c.3020A>C	ENSP00000417980.1:p.Glu1007Ala
ENST00000462942.3:c.1877A>C	ENSP00000436107.1:p.Glu626Ala
ENST00000486164.5:c.707A>C
ENST00000488242.2:n.546A>C
NM_024757.4:c.3020A>C	NP_079033.4:p.Glu1007Ala
XM_005266105.3:c.3011A>C	XP_005266162.1:p.Glu1004Ala
XM_005266110.1:c.2927A>C	XP_005266167.1:p.Glu976Ala
XM_006717288.2:c.3002A>C	XP_006717351.1:p.Glu1001Ala
XM_011519021.1:c.3029A>C	XP_011517323.1:p.Glu1010Ala
XM_011519022.1:c.3026A>C	XP_011517324.1:p.Glu1009Ala
XM_011519023.1:c.3008A>C	XP_011517325.1:p.Glu1003Ala
XM_011519024.1:c.2951A>C	XP_011517326.1:p.Glu984Ala
XM_011519025.1:c.2927A>C	XP_011517327.1:p.Glu976Ala
XM_011519026.1:c.2885A>C	XP_011517328.1:p.Glu962Ala
XM_011519029.1:c.1451A>C	XP_011517331.1:p.Glu484Ala
XM_011519030.1:c.803A>C	XP_011517332.1:p.Glu268Ala
XM_011519031.1:c.590A>C	XP_011517333.1:p.Glu197Ala
XM_011519032.1:c.590A>C	XP_011517334.1:p.Glu197Ala
XM_011519033.1:c.2864A>C	XP_011517335.1:p.Glu955Ala
NM_001354263.1:c.2999A>C	NP_001341192.1:p.Glu1000Ala
XM_005266105.5:c.3011A>C	XP_005266162.1:p.Glu1004Ala
XM_011519021.3:c.3029A>C	XP_011517323.1:p.Glu1010Ala
XM_011519022.3:c.3026A>C	XP_011517324.1:p.Glu1009Ala
XM_011519023.3:c.3008A>C	XP_011517325.1:p.Glu1003Ala
XM_011519029.3:c.1451A>C	XP_011517331.1:p.Glu484Ala
XM_011519030.3:c.803A>C	XP_011517332.1:p.Glu268Ala
XM_017015134.1:c.3005A>C	XP_016870623.1:p.Glu1002Ala
XM_017015136.2:c.2921A>C	XP_016870625.1:p.Glu974Ala
XM_017015137.1:c.2906A>C	XP_016870626.1:p.Glu969Ala
XM_017015138.1:c.2906A>C	XP_016870627.1:p.Glu969Ala
XM_024447674.1:c.2849A>C	XP_024303442.1:p.Glu950Ala
XM_024447675.1:c.2783A>C	XP_024303443.1:p.Glu928Ala
XM_024447676.1:c.2144A>C	XP_024303444.1:p.Glu715Ala
XM_024447677.1:c.2144A>C	XP_024303445.1:p.Glu715Ala
XM_024447680.1:c.2762A>C	XP_024303448.1:p.Glu921Ala
NM_024757.5:c.3020A>C MANE Select	NP_079033.4:p.Glu1007Ala
NM_001354263.2:c.2999A>C	NP_001341192.1:p.Glu1000Ala