Canonical Allele Identifier: CA468161041

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140707503A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137813051A>G , CM000671.2:g.137813051A>G	GRCh38
NC_000009.11:g.140707503A>G , CM000671.1:g.140707503A>G	GRCh37
NC_000009.10:g.139827324A>G	NCBI36
NG_011776.1:g.199060A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.2913A>G MANE Select	ENSP00000417980.1:p.Glu971=
ENST00000636027.1:c.2799A>G	ENSP00000489961.1:p.Glu933=
ENST00000637161.1:c.2820A>G	ENSP00000490328.1:p.Glu940=
ENST00000637261.1:c.2953A>G	ENSP00000490815.1:n.2953A>G
ENST00000637891.1:c.807A>G	ENSP00000490907.1:p.Glu269=
ENST00000460843.5:c.2913A>G	ENSP00000417980.1:p.Glu971=
ENST00000462942.3:c.1770A>G	ENSP00000436107.1:p.Glu590=
ENST00000486164.5:c.600A>G
ENST00000488242.2:n.439A>G
NM_024757.4:c.2913A>G	NP_079033.4:p.Glu971=
XM_005266105.3:c.2904A>G	XP_005266162.1:p.Glu968=
XM_005266110.1:c.2820A>G	XP_005266167.1:p.Glu940=
XM_006717288.2:c.2895A>G	XP_006717351.1:p.Glu965=
XM_011519021.1:c.2922A>G	XP_011517323.1:p.Glu974=
XM_011519022.1:c.2919A>G	XP_011517324.1:p.Glu973=
XM_011519023.1:c.2901A>G	XP_011517325.1:p.Glu967=
XM_011519024.1:c.2844A>G	XP_011517326.1:p.Glu948=
XM_011519025.1:c.2820A>G	XP_011517327.1:p.Glu940=
XM_011519026.1:c.2778A>G	XP_011517328.1:p.Glu926=
XM_011519029.1:c.1344A>G	XP_011517331.1:p.Glu448=
XM_011519030.1:c.696A>G	XP_011517332.1:p.Glu232=
XM_011519031.1:c.483A>G	XP_011517333.1:p.Glu161=
XM_011519032.1:c.483A>G	XP_011517334.1:p.Glu161=
XM_011519033.1:c.2757A>G	XP_011517335.1:p.Glu919=
NM_001354263.1:c.2892A>G	NP_001341192.1:p.Glu964=
XM_005266105.5:c.2904A>G	XP_005266162.1:p.Glu968=
XM_011519021.3:c.2922A>G	XP_011517323.1:p.Glu974=
XM_011519022.3:c.2919A>G	XP_011517324.1:p.Glu973=
XM_011519023.3:c.2901A>G	XP_011517325.1:p.Glu967=
XM_011519029.3:c.1344A>G	XP_011517331.1:p.Glu448=
XM_011519030.3:c.696A>G	XP_011517332.1:p.Glu232=
XM_017015134.1:c.2898A>G	XP_016870623.1:p.Glu966=
XM_017015136.2:c.2814A>G	XP_016870625.1:p.Glu938=
XM_017015137.1:c.2799A>G	XP_016870626.1:p.Glu933=
XM_017015138.1:c.2799A>G	XP_016870627.1:p.Glu933=
XM_024447674.1:c.2742A>G	XP_024303442.1:p.Glu914=
XM_024447675.1:c.2676A>G	XP_024303443.1:p.Glu892=
XM_024447676.1:c.2037A>G	XP_024303444.1:p.Glu679=
XM_024447677.1:c.2037A>G	XP_024303445.1:p.Glu679=
XM_024447680.1:c.2655A>G	XP_024303448.1:p.Glu885=
NM_024757.5:c.2913A>G MANE Select	NP_079033.4:p.Glu971=
NM_001354263.2:c.2892A>G	NP_001341192.1:p.Glu964=