Canonical Allele Identifier: CA468161023

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140707470T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137813018T>G , CM000671.2:g.137813018T>G	GRCh38
NC_000009.11:g.140707470T>G , CM000671.1:g.140707470T>G	GRCh37
NC_000009.10:g.139827291T>G	NCBI36
NG_011776.1:g.199027T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.2880T>G MANE Select	ENSP00000417980.1:p.Ser960=
ENST00000636027.1:c.2766T>G	ENSP00000489961.1:p.Ser922=
ENST00000637161.1:c.2787T>G	ENSP00000490328.1:p.Ser929=
ENST00000637261.1:c.2920T>G	ENSP00000490815.1:n.2920T>G
ENST00000637891.1:c.774T>G	ENSP00000490907.1:p.Ser258=
ENST00000460843.5:c.2880T>G	ENSP00000417980.1:p.Ser960=
ENST00000462942.3:c.1737T>G	ENSP00000436107.1:p.Ser579=
ENST00000486164.5:c.567T>G
ENST00000488242.2:n.406T>G
NM_024757.4:c.2880T>G	NP_079033.4:p.Ser960=
XM_005266105.3:c.2871T>G	XP_005266162.1:p.Ser957=
XM_005266110.1:c.2787T>G	XP_005266167.1:p.Ser929=
XM_006717288.2:c.2862T>G	XP_006717351.1:p.Ser954=
XM_011519021.1:c.2889T>G	XP_011517323.1:p.Ser963=
XM_011519022.1:c.2886T>G	XP_011517324.1:p.Ser962=
XM_011519023.1:c.2868T>G	XP_011517325.1:p.Ser956=
XM_011519024.1:c.2811T>G	XP_011517326.1:p.Ser937=
XM_011519025.1:c.2787T>G	XP_011517327.1:p.Ser929=
XM_011519026.1:c.2745T>G	XP_011517328.1:p.Ser915=
XM_011519029.1:c.1311T>G	XP_011517331.1:p.Ser437=
XM_011519030.1:c.663T>G	XP_011517332.1:p.Ser221=
XM_011519031.1:c.450T>G	XP_011517333.1:p.Ser150=
XM_011519032.1:c.450T>G	XP_011517334.1:p.Ser150=
XM_011519033.1:c.2724T>G	XP_011517335.1:p.Ser908=
NM_001354263.1:c.2859T>G	NP_001341192.1:p.Ser953=
XM_005266105.5:c.2871T>G	XP_005266162.1:p.Ser957=
XM_011519021.3:c.2889T>G	XP_011517323.1:p.Ser963=
XM_011519022.3:c.2886T>G	XP_011517324.1:p.Ser962=
XM_011519023.3:c.2868T>G	XP_011517325.1:p.Ser956=
XM_011519029.3:c.1311T>G	XP_011517331.1:p.Ser437=
XM_011519030.3:c.663T>G	XP_011517332.1:p.Ser221=
XM_017015134.1:c.2865T>G	XP_016870623.1:p.Ser955=
XM_017015136.2:c.2781T>G	XP_016870625.1:p.Ser927=
XM_017015137.1:c.2766T>G	XP_016870626.1:p.Ser922=
XM_017015138.1:c.2766T>G	XP_016870627.1:p.Ser922=
XM_024447674.1:c.2709T>G	XP_024303442.1:p.Ser903=
XM_024447675.1:c.2643T>G	XP_024303443.1:p.Ser881=
XM_024447676.1:c.2004T>G	XP_024303444.1:p.Ser668=
XM_024447677.1:c.2004T>G	XP_024303445.1:p.Ser668=
XM_024447680.1:c.2622T>G	XP_024303448.1:p.Ser874=
NM_024757.5:c.2880T>G MANE Select	NP_079033.4:p.Ser960=
NM_001354263.2:c.2859T>G	NP_001341192.1:p.Ser953=